Clinical trial Recruiting at 1 site Interventional Ages 6 to 12

Effects of PNF and Task-Oriented Training on Upper-Limb Function in Children with Spastic Diplegic Cerebral Palsy

Official title: Isolated Versus Combined Effects of Proprioceptive Neuromuscular Facilitation and Task-Oriented Training on Upper Extremity Function in Children With Spastic Diplegic Cerebral Palsy

Run by Ibadat International University, Islamabad · NCT07694804 · Data updated 2026-11-12

This study tests whether Proprioceptive Neuromuscular Facilitation (PNF), Task-Oriented Training (TOT), or both together can improve upper-extremity function in children with spastic diplegic cerebral palsy.

Quick facts

Study typeInterventional
Ages6 Years to 12 Years
SexAll
Enrollment63 (estimated)
SponsorIbadat International University, Islamabad
Academic / other
Locations1 site (Mansehra, KPK)
StatusRecruiting
StartedFebruary 17, 2026
Main results expectedJuly 5, 2026
Study endsJuly 8, 2026
Registry record updatedJuly 13, 2026
Trial IDNCT07694804 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are children aged 6–12 with spastic diplegic CP (GMFCS I–III) who can follow simple instructions and participate in physiotherapy.

Probably not a fit

Children with more severe upper-extremity contractures, uncontrolled epilepsy, or those unable to participate in therapy may receive limited or no benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this three-arm randomized trial, 63 children aged 6–12 with spastic diplegic CP (GMFCS I–III) will be assigned to PNF alone, TOT alone, or a combination of PNF and TOT. Each group will receive supervised 45-minute sessions, three times weekly for six weeks, focusing on improving coordination, motor control, and functional hand use. The study aims to compare the effects of the individual and combined interventions on upper extremity function and functional independence. The trial addresses a gap in evidence regarding how these rehabilitation approaches work alone versus together in this population. Outcomes will inform rehabilitation strategies to enhance participation in daily activities for children with CP.

Why it matters

Potential benefit: If successful, participants may experience improved upper-extremity function and greater independence in daily activities.

How similar studies have gone: Previous work suggests benefits from both PNF and TOT in CP, but direct comparisons and combination effects in spastic diplegic CP remain limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Children aged 6 to 12 years.
* Clinical diagnosis of spastic diplegic cerebral palsy.
* Gross Motor Function Classification System (GMFCS) Levels I-III.
* Ability to understand and follow simple verbal instructions.
* Medically stable and able to participate in physiotherapy sessions.
* Parent or legal guardian willing to provide written informed consent.

Exclusion Criteria:

* Orthopedic surgery involving the upper or lower extremities within the previous 6 months.
* Botulinum toxin injections administered within the previous 6 months.
* Severe visual, hearing, or cognitive impairments that would interfere with assessment or treatment.
* Uncontrolled epilepsy or other unstable neurological or medical conditions.
* Fixed upper extremity contractures or musculoskeletal deformities preventing participation in the intervention.
* Participation in another structured upper extremity rehabilitation program during the study period.
* Failure to obtain informed consent from a parent or legal guardian.

Where it's running

  • Helping Hand Institute of Rehabilitation
    Mansehra, Kpk, Pakistan
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.