- Study protocol
- Open Access
LEARN 2 MOVE 2-3: a randomized controlled trial on the efficacy of child-focused intervention and context-focused intervention in preschool children with cerebral palsy
BMC Pediatrics volume 10, Article number: 80 (2010)
Little is known about the efficacy and the working mechanisms of physical and occupational therapy interventions for children with cerebral palsy (CP). In recent years a shift from a child-focused intervention approach to a more context-focused intervention approach can be recognized. Until now the evidence on the efficacy and the working mechanisms of these interventions for children with CP is inconclusive. This study aims to evaluate the efficacy and working mechanisms of two intervention approaches compared to regular care intervention in improving mobility and self-care skills of children (2-3 years) with CP and their families: a child-focused intervention approach and a context-focused intervention approach.
A multi-centre, randomized controlled trial research design will be used. Ninety-four children with CP (Gross Motor Function Classification System (GMFCS) level I-IV; age 2 to 3 years), their parents, and service providers (physical and occupational therapists) will be included. During a period of six months children will receive child-focused, context-focused or regular care intervention. Therapists will be randomly assigned to deliver either a child-focused intervention approach, a context-focused intervention approach or regular care intervention. Children follow their therapist into the allocated intervention arm. After the six months study-intervention period, all participants return to regular care intervention. Outcomes will be evaluated at baseline, after six months and at a three months follow-up period. Primary outcome is the capability of functional skills in self-care and mobility, using the Functional Skills Scale of the Pediatric Evaluation of Disability Inventory (PEDI). Other outcomes will be quality of life and the domains of the International Classification of Functioning, Disability and Health - for Children and Youth (ICF-CY), including body function and structure, activities (gross motor capacity and performance of daily activities), social participation, environmental variables (family functioning, parental empowerment).
This paper presents the background information, design, description of interventions and protocol for this study on the efficacy and working mechanisms of child-focused intervention approach and context-focused intervention approach compared to regular care intervention in mobility and self-care skills of children (2-3 years) with CP.
This study is registered in the Dutch Trial Register as NTR1900
The present paper describes the background and design of LEARN 2 MOVE 2-3 (L2M 2-3). This project is part of the Dutch national LEARN 2 MOVE research program, which evaluates interventions in rehabilitation for children and adolescents with Cerebral Palsy (CP) in different age cohorts [1–3].
For children with CP at young age in general a shift from a child-focused intervention approach to a more context-focused intervention approach can be recognized. Until now however, the evidence on the efficacy and the working mechanisms of these intervention approaches for children with CP are inconclusive. Moreover, it is not known which interventions are being used in clinical practice, and how these developments transfer into clinical practice. L2M 2-3 focuses on these questions.
The child-focused intervention approach and context-focused intervention approaches are based on different principles as can be described in terms of the International Classification of Functioning, Disability and Health (ICF;) and the recently published derived version of it, the International Classification of Functioning, Disability and Health for Children and Youth (ICF-CY;). In the ICF and ICF-CY a persons functioning can be described on various levels (Figure 1) in its relation with environmental and personal factors.
Both the child-focused intervention approach and the context-focused intervention approach aim to improve activities and participation of the children. They differ however in the assumed pathways how to reach the goals at the level of activities and participation.
The child-focused intervention approach focuses primarily on remediation of body function and structure as the starting point of intervention. Interventions based on such an approach include: facilitation of normal movement patterns and postural control through physical handling [6–8], maintaining range of motion and joint alignment through stretching, casting and splinting [9, 10], strength training [11–13], and treadmill training . These strategies, focusing on remediation of body function and structure, can be performed in isolation or as part of practicing activities.
The context-focused intervention approach focuses primarily on changing constraints in the environment or task as the starting point of intervention. Both the physical environment and the social environment of the child are emphasized . In the context-focused intervention approach the therapist will not elicit specific responses by handling the child, but will provide an environment that enables the child to learn to perform self-initiated actions within naturally occurring restraints. The child can then become an active problem solver throughout the day instead of being a passive recipient of treatment. The social context of the child, especially the family, plays an important role.
Currently, CanChild Centre for Childhood Disability Research in Canada is performing a study into the efficacy of a child-focused intervention approach compared to a context-focused intervention approach, the Focus on Function Study . L2M 2-3 builds on the Focus on Function study in the way that the efficacy of the same child-focused intervention approach and context-focused intervention approach will be compared with the same outcome measures in different countries, and by adding the comparison with regular care. Little is known about the actual content of current interventions for young children with CP. They probably consist of a mix between the child-focused intervention approach and the context-focused intervention approach, without a clear theoretical base. To provide children with CP with the best intervention, it is necessary to understand which interventions are effective and why these interventions are effective.
The aim of the present project is to evaluate the efficacy of a child-focused intervention approach or a context-focused intervention approach versus regular care intervention in improving daily functioning of children (2-3 years) with CP and their families. In defining daily functioning it is important to distinguish three constructs of activity: capacity, capability, and performance. Capacity describes what a person can do in a standardized, controlled environment. Capability describes what a person can do in his/her daily environment. Performance describes what a person actually does do in his/her daily environment [17, 18].
Primary outcome in the present study is the capability of functional skills in self-care and mobility, as reflected in the first research question. Other domains and concepts of the ICF-CY are secondary outcomes, leading to the following research questions. Which of the three intervention approaches results in:
greater achievement of capability in functional skills in mobility and self-care of the children?
greater independence in the performance of mobility and self-care of the children?
greater achievement of capacity of motor skills of the children in a standardized environment?
greater participation of children and their families?
better quality of life of the children and their families?
In addition to the questions on efficacy, the working mechanisms of the child-focused intervention approach and the context-focused intervention approach will be examined. Parental stress, empowerment and family-centeredness of care will be analyzed in the three intervention groups. Moreover, variables that might be related to the efficacy of the intervention approaches and that might explain possible variability between children will be examined. In a longitudinal study of our research group on the development and determinants of daily activities in children with CP named PERRIN (Pediatric Rehabilitation Research in the Netherlands), and from recent literature, insight has been gained in child- and family-variables that possibly explain more about the working mechanisms of the interventions. These variables are: gross motor abilities [19, 20], manual abilities [21, 22], cognition of the child [21, 23, 24], and coping style of the parents [25–27]. We will collect data on these variables to get more insight in possible variability between children. Moreover, to get more insight into the working-mechanisms of the intervention approaches, part of the parents will be interviewed on their experiences with the interventions and therapists will be asked about preferences for intervention.
A multi-centre, randomized controlled trial research design will be used. The study protocol is approved by the Medical Ethics Committee of the University Medical Centre Utrecht, the Netherlands.
The study is a multi centre study and will be conducted in approximately 15 rehabilitation centers in the Netherlands between September 2009 to December 2011.
Ninety-four children with CP will be included. The inclusion criteria are:
Children with diagnosis of CP ;
Children enrolled in pediatric rehabilitation care, with at least physical or occupational therapy;
Children receiving therapy with a frequency of at least three sessions per month;
Children aged 24 months to 47 months (2-3 years) at the time of recruitment.
The exclusion criteria are:
Children with planned surgery or medical changes during the study that may affect their motor function;
Children whose families feel uncomfortable or unable to respond to interviews and questionnaires in Dutch (the language of all the study materials);
Since this an efficacy study, parents who state that they will not be able to adhere to one or two of the intervention approaches or to the treatment schedule, will not be entered in the study.
Children and their parents will be approached by their treating pediatric physician. They will receive an information letter, an informed consent form, a brochure about the LEARN 2 MOVE 2-3 study, and a brochure about participating in scientific research. The researcher will contact the parents after two weeks to respond to possible queries and provide additional information when necessary. Children of parents who give informed consent will participate in the study.
Sample size was calculated for the Pediatric Evaluation of Disability Inventory (PEDI) (based on data from an earlier study ; with a subgroup analysis of children of 2-3 years) using the following assumptions in a one-way analysis of variance power analysis (based on a power of 80% and a two-sided α-value of 0.05). An estimated difference in the change scores between the context-focused intervention approach group and the regular care intervention group of 4.5 points (SD = 6.0) on the PEDI. Sigma for the three groups = 2.1. Taking into account the clustered nature of the sample of participating children a correction will be used, based on an average cluster size (number of children per therapist) of 2, and an ICC of 0.1. These specifications lead to a required total sample size of 85. Expecting a 10% drop-out in total 94 children will be recruited for the present study.
The three interventions arms will be distributed within a centre. The physical and occupational therapists who agreed to participate will be randomized in one of the three intervention arms by block randomization, with a block size of six. Children will follow their therapist into the intervention group that the therapist was assigned to. The therapist who provides the study intervention to the child will be the prime therapist for the children during the six months study-intervention period. Furthermore, the prime therapist is the one who will document on the session documentation, will set goals with parents and is the contact person for the researchers. The other therapists who treat the child will be available for expert information consultation. Therapists can participate in the study with a maximum of two children at the same time and with a maximum of four children overall in the study. We expect an average of two children per therapist.
The study procedure for the participants is represented in Figure 2. After randomization procedures, therapists in the child-focused intervention approach and therapists in the context-focused intervention approach group will receive additional training. This training will start with both groups together (introduction and background of the study, and steps in discussing and formulating problems and goals with parents using the Canadian Occupational Performance Measure (COPM;) and Goal Attainment Scaling (GAS;). The second part of the training will be completed separately for each group and focuses on implementing the specific components of child-focused intervention approach or context-focused intervention approaches. Expert consultation will be available for therapists in each intervention group. The researchers and the consultant for each intervention will conduct the training sessions, providing both theoretical and applied information about the assessment and intervention protocols. Therapists will discuss case scenarios, and view videos of children. The training and training syllabus are developed based on materials from the Focus on Function study of CanChild. During the study therapists in the child-focused intervention approach and context-focused intervention approach groups will document sessions on standardized forms, and in the stage of goal-setting, will make a videotape of the child to make clear what the goals of the individual child and the parents are. The therapists will receive feedback on the session documentation and the video-tape which they send to the researchers. The therapists will have access to a consultant and the researchers, for support, problem solving, and resources. Therapists in the regular care intervention arm will be asked to work the way they are used to do, and at the end of the study their session documentation will be collected.
After inclusion in the study a baseline measurement (T0) will take place. Children will be assessed and parents will fill out questionnaires and will be interviewed on the measures as described in the Section Study Parameters. Parents can choose whether they would like to fill out the questionnaires on a digital or a paper version. Thereafter participants will follow their therapist into one of the three intervention groups for a six months study-intervention period. After these six months the second measurement (T1) will take place, after which all participants return to regular care intervention. At a three months follow-up period the third measurement (T2) will take place. Independent assessors who are blind for intervention allocation will asses the children and their parents.
Children included in the study typically receive physiotherapy and/or occupational therapy with a frequency of at least three times a month. During the six months study-intervention period, all children will receive at least 18 sessions of intervention. The amount of intervention sessions will be documented in the session documentation of the therapists.
In the child-focused intervention approach and context-focused intervention approach the procedure of problem definition, priorities, goals, analysis, sub goals and evaluation will be the same as much as possible, to avoid a confounding effect by procedure (see Table 1).
To ensure that the procedures in the child-focused intervention approach and the context-focused intervention approach are the same, forms will be used to guide the steps.
The child-focused intervention approach focuses primarily on remediation of body function and structure as the starting point of intervention. The task analysis focuses on constraints and facilitators in the child. Therapeutic techniques will be used to improve the child's body functions and structure, such as strength, coordination, balance, quality of movement, and range of motion. Strategies, focusing on remediation of body function and structure, can be performed in isolation or as part of practicing activities. The therapist is the primary decision maker in the intervention.
In the training therapists will learn child-focused intervention principles. Therapists will be instructed to achieve the goals primarily through changing the components of body function and structure within the child.
The context-focused intervention approach focuses primarily on changing constraints in the environment or task as the starting point of intervention. The task analysis focuses on constraints and facilitators in the environment and the task. For young children with CP (2-3 years) the most important contextual factors are situated in the home environment. In this approach therefore, the home environment is taken into consideration , and there is a strong collaboration between therapists and parents recognizing parents' role as advocates and decision makers for their child [35, 36]. In this approach, the task of the therapist is not to elicit specific responses by handling the child, but to provide an environment which enables the child to learn to perform self-initiated actions within naturally occurring restraints.
In the training the therapists will learn the context-focused intervention principles. Therapists will be instructed to achieve the goals primarily through changing the environment and tasks. Therefore, the therapists will challenge the children with frequent and varied practice within the context of daily activities and routines.
The regular care intervention in this study will be like the intervention the children received before participating in the study and continues throughout the study period. Regular care consists probably of a mixture of child-focused intervention approaches and context-focused intervention approaches, with the balance between child-focused and context-focused approaches based on the individual therapist's view.
Primary study outcome
The primary outcome of the study will be the capability of functional skills in mobility and self-care using the Functional Skills Scale of the PEDI (PEDI-FSS;). The PEDI is a standardized assessment instrument using parental reports through structured interview, and consists of the Functional Skills Scale (FSS), and the Caregiver Assistance Scale (CAS), both consisting of three domains: self-care, mobility, and social function. For the purpose of the present study the self-care and mobility domain will be used. The PEDI-FSS assesses what a child can do in his/her daily environment. Each question is scored as positive (score 1) or negative (score 0). A positive score is given when the child is capable of accomplishing the activity. The Dutch adaptation and translation of the PEDI, the PEDI-NL, which has good psychometric properties, will be used .
Secondary study outcomes
Performance of mobility-related activities and self-care-related activities will be measured by the Caregiver Assistance Scale of the PEDI (PEDI-CAS;). This scale measures the level of caregiver assistance a child receives to accomplish the activities. It concerns the child's actual behavior in his or her daily environment.
To set intervention goals and to measure the amount of successfully reached goals after the six months study-intervention period the COPM will be used . The COPM is an individualized measure designed to detect problems in various areas of daily functioning and to assess changes in self-perceived performance and satisfaction over time through a semi-structured interview. The COPM has robust psychometric properties for use in a pediatric clinical trial . The Dutch version of the COPM has shown good validity [41, 42].
Capacity of motor skills will be assessed with the Gross Motor Function Measure (GMFM;). The GMFM is a standardized observational instrument that has been developed to measure the gross motor function in children with CP in a specific test situation, without the use of mobility aids or orthosis. The original GMFM consists of 88 items grouped into five dimensions of gross motor function: lying and rolling; sitting; crawling and kneeling; standing; and walking, running, and jumping. There is also a 66-item version of the GMFM available, in which 22 items of the GMFM-88 are removed, many of them in the dimension of lying and rolling. The most recent development with the GMFM is the GMFM-66-IS (Item-Set) in which four items sets are used to determine which items need to be examined. This abbreviated version of the GMFM is less time consuming and has shown to be valid en reliable . In the present study, with a study population of children with CP aged 2 to 3 years, we expect that the lying and rolling and sitting dimensions can provide essential information. Therefore all items of these two dimensions of the GMFM-88 will be assessed. In addition the GMFM-66-IS will be used to determine which items on the other dimensions need to be examined for each individual child. The Dutch translation of the GMFM-88, which has good psychometric properties comparable to those of the original GMFM will be used [45, 46].
Participation of the child in daily life activities will be measured by the Preschool Children's Assessment of Participation and Enjoyment (Pre-School CAPE). The Pre-school CAPE is a measure based on the CAPE (Children's Assessment of Participation and Enjoyment) . The CAPE is a self-reported 55-item questionnaire to measure participation and enjoyment in children 6 to 21 years of age. The CAPE has shown to be sensitive in measuring change in participation during intervention  and shows good psychometric properties [35, 49]. The CAPE was adapted for children at a younger age to the Pre-school CAPE by changing some items and parents will fill in the questionnaire for their children. This questionnaire consists of 48 items to measure the participation in everyday activities in children over the past four months. The Pre-school CAPE measures on five domains: play activities, skill development, active physical recreation, social activities and other activities. The questionnaire provides information on the diversity and intensity of these activities.
Parental perception of the participation of the family will be measured by the Family participation questionnaire. In a semi-structured interview parents are asked three questions on daily activities of the family, and on family participation. The questionnaire has shown shows good inter-rater reliability in the PERRIN CP 0-5 study.
Quality of life of the child will be measured by TNO-AZL Preschool Children Quality of Life Questionnaire (TAPQOL;). The TAPQOL is a 43-item questionnaire to measure parents' perception of the health-related quality of life in preschool children. Parents fill in the questionnaire as a proxy for their child. The questionnaire consists of 12 scales on the domain of physical, social, cognitive and emotional functioning. The occurrence of these items is assessed and at some items also the wellbeing of the child in relation to the item is scored. The TAPQOL showed to have a good reliability [51, 52].
Quality of life of the parents will be measured by three questions based on a national survey of 'Statistics Netherlands', the Questions Quality of Life. The answers of these questions can be compared with Dutch norms.
Parental stress in relation to raising their child will be measured by the Nijmeegse Ouderlijke Stress Index - Kort (NOSI-K;). The NOSI-K is with 25 items the short version of the NOSI, which is a Dutch adaptation of the Parenting Stress Index (PSI). The NOSI-K has shown good psychometric properties .
The empowerment of the family will be measured by the Family Empowerment Scale (FES;). The FES is a 34-item questionnaire to measure empowerment in families of children with emotional, behavioral or mental disorders. The FES consists of three domains about family, child's services, and parents' involvement in the community. The FES has good psychometric properties [54, 55].
The family-centeredness of care as rated by the parents will be measured by the Measure of Processes of Care (MPOC;). The MPOC is a 56-item questionnaire to assess the extent to which parents perceived the family centeredness of the health care their child received in the past year. The questionnaire consists of five scales; enabling and partnership, providing general information, providing specific information about the child, coordinated and comprehensive care for the child and family, and respectful and supportive care. The occurring of these items will be assessed as well as how important they are to parents. In this study the Dutch version of the MPOC will be used, with good psychometric properties .
The family-centeredness of care as rated by professionals will be measured by the Measure of Processes of Care for service providers (MPOC-SP;). The MPOC-SP is a 27-item questionnaire to assess to which extent the care that service providers provided the past year was family-centered. The questionnaire consists of four scales. In this study the Dutch version of the MPOC-SP will be used, with good psychometric properties [58, 59].
Other study parameters
Based on the literature, it is assumed that some child- and family variables might be important in explaining effects in different groups. Therefore, the following variables will be registered systematically, and will be analyzed as potential determinants:
The gross motor ability level of the child will be classified by the GMFCS [29, 30]. The GMFCS is a classification system based on the self-initiated movements of the child. The system consists of a 5-level ordinal scale, which describes differences in severity of mobility abilities. Level I represents the best gross motor function, level V the least. The GMFCS shows good psychometric properties [29, 30].
Manual skills will be classified by the Manual Ability Classification System (MACS; ). The classification system consists of five levels, from level I 'Handles objects easily and successfully' to level V 'Does not handle objects and has severely limited ability to perform even simple actions'. The MACS has shown good reliability in children 2-5 years of age . Validity of the MACS was shown in children 4-18 years of age . The validity in children 2-5 years of age has not been studied yet.
Type of CP will be classified according to Surveillance of Cerebral Palsy in Europe (SCPE) - guideline . This guideline classifies CP in the subtypes of spastic, dyskinetic, or ataxic. Also the topographical distribution is classified in children with spastic CP; unilateral involvement (hemiplegia) versus bilateral involvement (diplegia, tetraplegia).
Cognitive functioning of the child will be measured by the Bayley Scales of Infant Development-Second edition (BSID-II) - Mental Scale, with good psychometric properties .
Coping style of the parents will be measured by the Utrechtse Copinglijst (UCL), a Dutch 47-item questionnaire to determine how parents handle problems and events in daily life, with sufficient psychometric properties .
Session documentation of the therapists will be collected. Therapists in the child-focused intervention approach and in the context-focused intervention approach group will document on special forms and will send in their documentation during the intervention period to control the therapist's adherence. Experience from previous work [31, 65, 66] has shown that therapists are able to implement treatment protocols in a reliable and valid manner. Therapists in the regular care intervention group will not receive instructions on documentation and will document the way they are used to do. Their documentation will be collected after the end of the study. Therapists in all groups will videotape one session of each child at four months of study-intervention. These tapes will be evaluated by trained raters, for procedural reliability and to describe regular care intervention.
Additional data on the working mechanisms will be collected by in-depth interviews with the families. Parents of children in the child-focused intervention approach and context-focused intervention approach group will be interviewed after the six months study-intervention period. Questions will be on parents experiences with the interventions, to get more insight into the advantages and disadvantages of the interventions. We expect that an 'informational redundancy'-effect will occur after interviewing half of the parents. To prevent that parents will be interviewed unnecessary, not all parents will be interviewed.
Descriptive statistics including frequencies, means, standard deviations, and for nonparametric data medians and interquartile ranges will be calculated. Data will be analyzed based on an intention to treat-analysis. The effects of the three interventions will be evaluated using repeated-measures analysis of variance (group × time) with the outcome measures as the dependent variable. In case of a statistically significant interaction group × time effect, post-hoc analyses will be performed to determine between which groups the differences occur. To assess the effects during and after the six month study-intervention period, repeated-measures analysis of variance (group × time) with repeated contrasts will be used, with the same outcome measures.
To explore variables that might be related to the efficacy of the intervention, and that might explain possible variability between children, multiple regression analyses will be performed. The change scores on the PEDI-FSS will be the dependent variable, and the classification of gross motor abilities, classification of manual abilities, cognition of the child and coping style of the parents will be analyzed as independent variables.
The interviews with the parents on their experiences with the interventions, and therapists' preferences for intervention will be analyzed using qualitative analyses.
To provide the best intervention promoting outcome in children with developmental disabilities, it is necessary to examine which interventions are effective in randomized controlled trials and to study why a specific intervention is effective. Little is known about the efficacy and the working mechanisms of physical and occupational therapy interventions for children with CP. In this paper we have presented the background information, design, description of interventions and protocol for this study on the efficacy and working mechanisms of child-focused intervention approach and context-focused intervention approach compared to regular care intervention in mobility and self-care skills of children (2-3 years) with CP.
Hielkema T, Hamer EG, Reinders-Messelink HA, Maathuis CGB, Bos AF, Dirks T, van Doormaal L, Verheijden JMA, Vlaskamp C, Lindeman E, Hadders-Algra M: LEARN 2 MOVE 0-2 years: effects of a new intervention program in infants at very high risk for cerebral palsy; a randomized controlled trial. BMC Pediatrics. 2010.
van Wely L, Becher JG, Reinders-Messelink HA, Lindeman E, Verschuren O, Verheijden JMA, Dallmeijer AJ: LEARN 2 MOVE 7-12 years: a randomized controlled trial on the effects of a physical activity stimulation program in children with cerebral palsy. BMC Pediatrics. 2010.
Slaman J, Roebroeck ME, van Meeteren J, van der Slot WM, Reinders-Messelink HA, Lindeman E, Stam HJ, van den Berg-Emons RJ: LEARN 2 MOVE 16-24: Effectiveness of an intervention to stimulate physical activity and improve physical fitness of adolescents and young adults with spastic cerebral palsy; a randomized controlled trial. BMC Pediatrics. 2010.
World Health Organization: International Classification of Functioning, Disability and Health. 2001, Geneva: WHO
World Health Organization: International Classification of Functioning, Disability and health version for children and Youth. 2004, Geneva: WHO
Brown GT, Burns SA: The Efficacy of Neurodevelopmental Treatment in Paediatrics: a Systematic Review. Br J Occup Ther. 2001, 64: 235-244.
Butler C, Darrah J: Effects of neurodevelopmental treatment (NDT) for cerebral palsy: an AACPDM evidence report. Dev Med Child Neurol. 2001, 43: 778-790. 10.1017/S0012162201001414.
Farmer SE, Butler PB, Major RE: Targeted Training for Crouch Posture in Cerebral Palsy: A case report. Physiotherapy. 1999, 85: 242-247. 10.1016/S0031-9406(05)61437-X.
Cottalorda J, Gautheron V, Metton G, Charmet E, Chavrier Y: Toe-walking in children younger than six years with cerebral palsy. The contribution of serial corrective casts. J Bone Joint Surg Br. 2000, 82: 541-544. 10.1302/0301-620X.82B4.10188.
Hainsworth F, Harrison MJ, Sheldon TA, Roussounis SH: A preliminary evaluation of ankle orthoses in the management of children with cerebral palsy 1. Dev Med Child Neurol. 1997, 39: 243-247. 10.1111/j.1469-8749.1997.tb07419.x.
Fowler EG, Ho TW, Nwigwe AI, Dorey FJ: The effect of quadriceps femoris muscle strengthening exercises on spasticity in children with cerebral palsy. Phys Ther. 2001, 81: 1215-1223.
Ross SA, Engsberg JR, Olree KS, Park TS: Quadriceps and Hamstring Strength Changes as a Function of Selective Dorsal Rhizotomy Surgery and Rehabilitation. Pediatr Phys Ther. 2001, 13: 2-9. 10.1097/00001577-200104000-00002.
Haney N: Muscle Strengthening in Children with Cerebral Palsy. Phys Occup Ther Pediatr. 1998, 18: 149-157.
Schindl MR, Forstner C, Kern H, Hesse S: Treadmill training with partial body weight support in nonambulatory patients with cerebral palsy. Arch Phys Med Rehabil. 2000, 81: 301-306. 10.1016/S0003-9993(00)90075-3.
Law M, Darrah J, Pollock N, King G, Rosenbaum P, Russell D, Palisano R, Harris S, Armstrong R, Watt J: Family-Centred Functional Therapy for Children with Cerebral Palsy: An Emerging Practice Model. Phys Occup Ther Pediatr. 1998, 18: 83-102.
Law M, Darrah J, Pollock N, Rosenbaum P, Russell D, Walter SD, Petrenchik T, Wilson B, Wright V: Focus on Function - a randomized controlled trial comparing two rehabilitation interventions for young children with cerebral palsy. BMC Pediatr. 2007, 7: 31-10.1186/1471-2431-7-31.
Holsbeeke L, Ketelaar M, Schoemaker MM, Gorter JW: Capacity, capability, and performance: different constructs or three of a kind?. Arch Phys Med Rehabil. 2009, 90: 849-855. 10.1016/j.apmr.2008.11.015.
Smits DW, Gorter JW, Ketelaar M, van Schie PE, Dallmeijer AJ, Lindeman E, Jongmans MJ: Relationship between gross motor capacity and daily-life mobility in children with cerebral palsy. Dev Med Child Neurol. 2010, 52: e60-66. 10.1111/j.1469-8749.2009.03525.x.
Voorman JM, Dallmeijer AJ, Schuengel C, Knol DL, Lankhorst GJ, Becher JG: Activities and participation of 9- to 13-year-old children with cerebral palsy. Clin Rehabil. 2006, 20: 937-948. 10.1177/0269215506069673.
Rosenbaum PL, Walter SD, Hanna SE, Palisano RJ, Russell DJ, Raina P, Wood E, Bartlett DJ, Galuppi BE: Prognosis for gross motor function in cerebral palsy: creation of motor development curves. JAMA. 2002, 288: 1357-1363. 10.1001/jama.288.11.1357.
Beckung E, Hagberg G: Neuroimpairments, activity limitations, and participation restrictions in children with cerebral palsy. Dev Med Child Neurol. 2002, 44: 309-316. 10.1111/j.1469-8749.2002.tb00816.x.
Morris C, Kurinczuk JJ, Fitzpatrick R, Rosenbaum PL: Do the abilities of children with cerebral palsy explain their activities and participation?. Dev Med Child Neurol. 2006, 48: 954-961. 10.1017/S0012162206002106.
Ostensjo S, Carlberg EB, Vollestad NK: Everyday functioning in young children with cerebral palsy: functional skills, caregiver assistance, and modifications of the environment. Dev Med Child Neurol. 2003, 45: 603-612. 10.1111/j.1469-8749.2003.tb00964.x.
Enkelaar L, Ketelaar M, Gorter JW: Association between motor and mental functioning in toddlers with cerebral palsy. Dev Neurorehabil. 2008, 11: 276-282. 10.1080/17518420802581164.
Rentinck IC, Ketelaar M, Jongmans MJ, Gorter JW: Parents of children with cerebral palsy: a review of factors related to the process of adaptation. Child Care Health Dev. 2007, 33: 161-169. 10.1111/j.1365-2214.2006.00643.x.
Ketelaar M, Volman MJ, Gorter JW, Vermeer A: Stress in parents of children with cerebral palsy: what sources of stress are we talking about?. Child Care Health Dev. 2008, 34: 825-829. 10.1111/j.1365-2214.2008.00876.x.
Schuengel C, Rentinck IC, Stolk J, Voorman JM, Loots GM, Ketelaar M, Gorter JW, Becher JG: Parents' reactions to the diagnosis of cerebral palsy: associations between resolution, age and severity of disability. Child Care Health Dev. 2009, 35: 673-680. 10.1111/j.1365-2214.2009.00951.x.
Rosenbaum P, Paneth N, Leviton A, Goldstein M, Bax M, Damiano D, Dan B, Jacobsson B: A report: the definition and classification of cerebral palsy April 2006. Dev Med Child Neurol Suppl. 2007, 109: 8-14.
Palisano R, Rosenbaum P, Walter S, Russell D, Wood E, Galuppi B: Development and reliability of a system to classify gross motor function in children with cerebral palsy. Dev Med Child Neurol. 1997, 39: 214-223. 10.1111/j.1469-8749.1997.tb07414.x.
Palisano RJ, Rosenbaum P, Bartlett D, Livingston MH: Content validity of the expanded and revised Gross Motor Function Classification System. Dev Med Child Neurol. 2008, 50: 744-750. 10.1111/j.1469-8749.2008.03089.x.
Ketelaar M, Vermeer A, Hart H, Beek Petegem-van, Helders PJ: Effects of a functional therapy program on motor abilities of children with cerebral palsy. Phys Ther. 2001, 81: 1534-1545.
Law M, Baptiste S, Carswell A, McColl MA, Polatajko H, Pollock N: Canadian Occupational Performance Measure. 1998, Ottawa, ON: CAOT Publications ACE, 2
Steenbeek D, Ketelaar M, Lindeman E, Galama K, Gorter JW: Interrater reliability of goal attainment scaling in rehabilitation of children with cerebral palsy. Arch Phys Med Rehabil. 2010, 91: 429-435. 10.1016/j.apmr.2009.10.013.
Palisano RJ: A collaborative model of service delivery for children with movement disorders: a framework for evidence-based decision making. Phys Ther. 2006, 86: 1295-1305. 10.2522/ptj.20050348.
King S, Teplicky R, King G, Rosenbaum P: Family-centered service for children with cerebral palsy and their families: a review of the literature. Semin Pediatr Neurol. 2004, 11: 78-86. 10.1016/j.spen.2004.01.009.
Palisano RJ, Snider LM, Orlin MN: Recent advances in physical and occupational therapy for children with cerebral palsy. Semin Pediatr Neurol. 2004, 11: 66-77. 10.1016/j.spen.2004.01.010.
Haley SM, Coster WJ, Ludlow LH, Haltiwanger JT, Andrellos PJ: Pediatric Evaluation of Disability Inventory: Development, standardization, and administration manual. 1992, Boston, MA: New England Medical Centre Inc. and PEDI Research Group ed
Wassenberg-Severijnen JE, Custers JW: Handleiding PEDI-NL. Amsterdam. 2005, Harcourt Test Publishers
Wassenberg-Severijnen JE, Custers JW, Hox JJ, Vermeer A, Helders PJ: Reliability of the Dutch Pediatric Evaluation of Disability Inventory (PEDI). Clin Rehabil. 2003, 17: 457-462. 10.1191/0269215503cr634oa.
Cusick A, Lannin NA, Lowe K: Adapting the Canadian Occupational Performance Measure for use in a paediatric clinical trial. Disabil Rehabil. 2007, 29: 761-766. 10.1080/09638280600929201.
Verkerk GJ, Wolf MJ, Louwers AM, Meester-Delver A, Nollet F: The reproducibility and validity of the Canadian Occupational Performance Measure in parents of children with disabilities. Clin Rehabil. 2006, 20: 980-988. 10.1177/0269215506070703.
Dedding C, Cardol M, Eyssen IC, Dekker J, Beelen A: Validity of the Canadian Occupational Performance Measure: a client-centred outcome measurement. Clin Rehabil. 2004, 18: 660-667. 10.1191/0269215504cr746oa.
Russell DJ, Rosenbaum PL, Cadman DT, Gowland C, Hardy S, Jarvis S: The gross motor function measure: a means to evaluate the effects of physical therapy. Dev Med Child Neurol. 1989, 31: 341-352. 10.1111/j.1469-8749.1989.tb04003.x.
Russell DJ, Avery LM, Walter SD, Hanna SE, Bartlett DJ, Rosenbaum PL, Palisano RJ, Gorter JW: Development and validation of item sets to improve efficiency of administration of the 66-item Gross Motor Function Measure in children with cerebral palsy. Dev Med Child Neurol. 2010, 52: e48-e54. 10.1111/j.1469-8749.2009.03481.x.
Veenhof C, Ketelaar M, Beek Petegem-van: De Gross Motor Function Measure (GMFM): Een onderzoek naar de responsiviteit van de Nederlandse vertaling. Ned T Fysiotherapie. 2003, 113: 36-41.
Veenhof C, Ketelaar M, Petegem-van Beek E: De Gross Motor Function Measure (GMFM): Een onderzoek naar de betrouwbaarheid van de Nederlandse vertaling. Ned Tijds Fysiother. 2003, 113: 32-35.
King G, King S, Rosenbaum P, Kertoy M, Law M, Hurley P, Hanna S, Young NL: CAPE/PAC; Children's Assessment of participation and Enjoyment & Preferences for Activities of Children. 2004, San Antonio: Harcourt Assessment
Verschuren O, Ketelaar M, Gorter JW, Helders PJ, Uiterwaal CS, Takken T: Exercise training program in children and adolescents with cerebral palsy: a randomized controlled trial. Arch Pediatr Adolesc Med. 2007, 161: 1075-1081. 10.1001/archpedi.161.11.1075.
King GA, Law M, King S, Hurley P, Hanna S, Kertoy M, Rosenbaum P: Measuring children's participation in recreation and leisure activities: construct validation of the CAPE and PAC. Child Care Health Dev. 2007, 33: 28-39. 10.1111/j.1365-2214.2006.00613.x.
Rentinck IC, Gorter JW, Ketelaar M, Lindeman E, Jongmans MJ: Perceptions of family participation among parents of children with cerebral palsy followed from infancy to toddler hood. Disabil Rehabil. 2009, 31: 1828-1834. 10.1080/09638280902822286.
Fekkes M, Theunissen NC, Brugman E, Veen S, Verrips EG, Koopman HM, Vogels T, Wit JM, Verloove-Vanhorick SP: Development and psychometric evaluation of the TAPQOL: a health-related quality of life instrument for 1-5-year-old children. Qual Life Res. 2000, 9: 961-972. 10.1023/A:1008981603178.
Bunge EM, Essink-Bot ML, Kobussen MP, van Suijlekom-Smit LW, Moll HA, Raat H: Reliability and validity of health status measurement by the TAPQOL. Arch Dis Child. 2005, 90: 351-358. 10.1136/adc.2003.048645.
de Brock AJJL, Vermulst AA, Gerris JRM: NOSI: Nijmeegse Ouderlijke Stress Index, Handleiding. 1992, Lisse: Swets & Zeitlinger
Koren PE, DeChillo N, Friesen BJ: Measuring empowerment in families whose children have emotional disabilities: A brief questionnaire. Rehabil Psychol. 1992, 37: 305-320. 10.1037/h0079106.
Singh NN, Curtis WJ: Psychometric analysis of the family empowerment scale. J Emot Behav Disord. 1995, 3: 85-10.1177/106342669500300203.
King SM, Rosenbaum PL, King GA: Parents' perceptions of caregiving: development and validation of a measure of processes. Dev Med Child Neurol. 1996, 38: 757-772. 10.1111/j.1469-8749.1996.tb15110.x.
Schie PEMv, Siebes RC, Ketelaar M, Vermeer A: The measure of processes of care (MPOC): validation of the Dutch Translation. Child Care Health Dev. 2004, 30: 529-539. 10.1111/j.1365-2214.2004.00451.x.
Siebes RC, Nijhuis BJ, Boonstra AM, Ketelaar M, Wijnroks L, Reinders-Messelink HA, Postema K, Vermeer A: A family-specific use of the Measure of Processes of Care for Service Providers (MPOC-SP). Clin Rehabil. 2008, 22: 242-251. 10.1177/0269215507081568.
Siebes RC, Ketelaar M, Wijnroks L, van Schie PE, Nijhuis BJ, Vermeer A, Gorter JW: Family-centred services in The Netherlands: validating a self-report measure for paediatric service providers. Clin Rehabil. 2006, 20: 502-512. 10.1191/0269215506cr979oa.
Eliasson AC, Krumlinde-Sundholm L, Rosblad B, Beckung E, Arner M, Ohrvall AM, Rosenbaum P: The Manual Ability Classification System (MACS) for children with cerebral palsy: scale development and evidence of validity and reliability. Dev Med Child Neurol. 2006, 48: 549-554. 10.1017/S0012162206001162.
Plasschaert VF, Ketelaar M, Nijnuis MG, Enkelaar L, Gorter JW: Classification of manual abilities in children with cerebral palsy under 5 years of age: how reliable is the Manual Ability Classification System?. Clin Rehabil. 2009, 23: 164-170. 10.1177/0269215508098892.
Surveillance of Cerebral Palsy in Europe (SCPE): Prevalence and characteristics of children with cerebral palsy in Europe. Dev Med Child Neurol. 2002, 44: 633-640. 10.1111/j.1469-8749.2002.tb00848.x.
Bayley N: Manual for the Bayley Scales of Infant Development. 1993, San Antonio: The Psychological Corporation
Schreurs PFG, van de Willige G, Brosschot JF, Tellegen B, Graus GMH: De Utrechtse Coping Lijst (The Utrecht Coping List): UCL. 1988, Lisse, The Netherlands: Swets en Zeitlinger BV
Law M, Cadman D, Rosenbaum P, Walter S, Russell D, DeMatteo C: Neurodevelopmental therapy and upper-extremity inhibitive casting for children with cerebral palsy. Dev Med Child Neurol. 1991, 33: 379-387. 10.1111/j.1469-8749.1991.tb14897.x.
Law M, Russell D, Pollock N, Rosenbaum P, Walter S, King G: A comparison of intensive neurodevelopmental therapy plus casting and a regular occupational therapy program for children with cerebral palsy. Dev Med Child Neurol. 1997, 39: 664-670. 10.1111/j.1469-8749.1997.tb07360.x.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2431/10/80/prepub
This project is part of the national LEARN 2 MOVE research program and is supported financially by ZonMw, Johanna Kinderfonds, Stichting Rotterdams Kinderrevalidatie Fonds Adriaanstichting, Revalidatiefonds, Phelps Stichting, Revalidatie Nederland and the Nederlandse Vereniging van Revalidatieartsen.
The authors declare that they have no competing interests.
MK and JG developed the original concept and wrote the grant application; all authors contributed to the design and the protocol of the study; MK, AK and OV are involved in the study implementation. EL is the program leader, and HR is the program coordinator of the research program LEARN 2 MOVE; MK is the project leader of LEARN 2 MOVE 2-3. All authors participated in the writing and or reviewing of this manuscript. All authors read and approved the final manuscript.
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Ketelaar, M., Kruijsen, A.J., Verschuren, O. et al. LEARN 2 MOVE 2-3: a randomized controlled trial on the efficacy of child-focused intervention and context-focused intervention in preschool children with cerebral palsy. BMC Pediatr 10, 80 (2010). https://doi.org/10.1186/1471-2431-10-80
- Cerebral Palsy
- Intervention Approach
- Good Psychometric Property
- Gross Motor Function Classification System
- Goal Attainment Scaling