NCT06532513 Family-Centered Physiotherapy in Dyskinetic Cerebral Palsy
| NCT ID | NCT06532513 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Hacettepe University |
| Condition | Cerebral Palsy, Dyskinetic |
| Study Type | INTERVENTIONAL |
| Enrollment | 24 participants |
| Start Date | 2024-10-15 |
| Primary Completion | 2025-05-15 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 24 participants in total. It began in 2024-10-15 with a primary completion date of 2025-05-15.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This study aimed to examine the impact of family centered, goal-oriented physiotherapy and rehabilitation on body function, activity, participation, and quality of life in severely affected children with dyskinetic cerebral palsy (DCP). The first assessment was conducted and recorded for all patients at the beginning of the study. Subsequently, the study group was taught family centered physiotherapy practices in addition to routine physiotherapy for 10 weeks to be performed at home. The control group only received routine physiotherapy. Weekly remote monitoring, regular meetings, and a second assessment at the 10th week were conducted. The study concluded with all face-to-face assessments. According to the research protocol, the primary aim of this study was to evaluate the effectiveness of a 10-week family centered physiotherapy application. The goal of this intervention was to improve movement and posture, thereby enhancing daily activities and quality of life. The primary endpoint of the study was to determine the impact of family physiotherapy application taught to families during the 10-week education period. This study was conducted at the Faculty of Physical Therapy and Rehabilitation, Hacettepe University. This study aimed to structure and define a family centered, goal-oriented, personalized physiotherapy, and rehabilitation application for the treatment of children with cerebral palsy. One of the significant objectives of this study was to examine the effects of this intervention within the framework of the International Classification of Functioning, Disability, and Health (ICF) on body function, activity, participation, and quality of life. The study protocol started with evaluations from patients after obtaining approval from the ethics committees. The study will be completed within a follow-up period of four months without treatment, including the remote monitoring process. The results of this study aimed to provide valuable information about the effectiveness of family centered physiotherapy application in severely affected children with dyskinetic cerebral palsy.
Eligibility Criteria
Inclusion Criteria: 1. Being in the age range of 5-18 years 2. Having a diagnosis of Dyskinetic Cerebral Palsy (DSP) confirmed by a pediatric neurologist 3. Being classified with a gross motor function level of IV-V using the Expanded and Revised Gross Motor Function Classification System (GMFCS E\&R) 4. Having a Manual Ability Classification System (MACS) classification of manual ability level IV-V 5. Having a Communication Function Classification System (CFCS) communication function level of I-II-III 6. For volunteers participating through Zoom and Whatsapp applications, having computer literacy and these applications installed on their devices e. Continuing routine physiotherapy and rehabilitation programs. Exclusion Criteria: 1. Having difficulty understanding and following instructions 2. Having severe visual impairments 3. Having undergone orthopedic or brain surgery interventions in the last 12 months.
Contact & Investigator
Ceren Günbey, PhD
STUDY DIRECTOR
Hacettepe University
Frequently Asked Questions
Who can join the NCT06532513 clinical trial?
This trial is open to participants of all sexes, aged 5 Years or older, up to 18 Years, studying Cerebral Palsy, Dyskinetic. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06532513 currently recruiting?
Yes, NCT06532513 is actively recruiting participants. Contact the research team at mintaze@hacettepe.edu.tr for enrollment information.
Where is the NCT06532513 trial being conducted?
This trial is being conducted at Ankara, Turkey (Türkiye).
Who is sponsoring the NCT06532513 clinical trial?
NCT06532513 is sponsored by Hacettepe University. The principal investigator is Ceren Günbey, PhD at Hacettepe University. The trial plans to enroll 24 participants.
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