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Effectiveness of Family-Professional Collaboration on Functional Goals Achievement of Children With Cerebral Palsy and Caregivers' Quality of Life and Burden

K

King Saud University

Status

Completed

Conditions

Collaborative Intervention Process
Cerebral Palsy
Functional Goals Achievement

Treatments

Other: family-professional collaboration practice model

Study type

Interventional

Funder types

Other

Identifiers

NCT05709080
IRB No.: 36-2020-IRB

Details and patient eligibility

About

The aim of this study is to examine the effect of implanting the family-professional collaboration practice model on the functional goals achievement of children with CP and their caregivers' quality of life and burden. The children will be treated by physical therapists who will be assigned to two groups (control and experimental).

Full description

A randomized, single-blinded control study involved 28 physical therapists and 44 pairs of children with CP aged 2-12 years old and their caregivers will be assigned randomly into experimental and control groups. Physical therapists in the experimental group will receive two instructional sessions (3 hours each) to implement collaboration during the therapy sessions and physical therapists in the control group will receive no instructions. Children will receive 45- 60 minutes therapy sessions (5 sessions/week) for six weeks. Goal Attainment Scaling (GAS) to measure the children's goals achievement change rate, the Arabic version of the World Health Organization Quality of Life Brief (WHOQOL- Brief) to examine the caregivers' quality of life, and the Zarit Burden Interview Arabic Abridged version (ZBI-A) to evaluate the caregivers' burden will be used.

Enrollment

54 patients

Sex

All

Ages

2 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Physical therapists with at least one year of experience in pediatric physical therapy.
  • Children with CP, aged between 2 to 12 years, Gross Motor Function Classification System (GMFCS) level I, II, and III, and attended the physical therapy sessions accompanied by their caregivers.

Exclusion criteria

  • Physical therapists in the experimental group who rate their level of confidence to implement the collaborative strategies less than 4 out of 5.
  • children who underwent recent surgery (6 months) or after Botulinum toxin injection treatment (3 months), had uncontrolled seizure disorder, or discontinued physical therapy sessions.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 2 patient groups

family-professional collaboration practice model
Experimental group
Description:
Physical therapists in the family-professional collaboration practice model group will receive instructions in the collaborative intervention, following the process and the strategies of the family-professional collaboration practice model to enhance the collaboration during physical therapy sessions. The instruction conducted online in two sessions for six hours (3 hours per session). the therapists in this group will treat the children according to steps of family-professional collaboration practice model: Step 1: Mutually agreed-upon goals, Step 2: shared planning, Step 3:Shared implementation, and Step 4: Shared evaluation of child and family outcomes.
Treatment:
Other: family-professional collaboration practice model
conventional therapy
No Intervention group
Description:
Physical therapists in the conventional therapy group will not receive any instructions related to the collaborative intervention process. the therapists in this group will treat the children as conventional therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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