Video-based Visual Feedback Combined With Task-oriented Physiotherapy Among Cerebral Palsy
Effects of Video-Based Visual Feeback Combined With Task-oriented Physiotherapy on Gross Motor Function, Balance, and Gait in Children With Spastic Cerebral Palsy
To determine the effects of Video-based visual feedback combined with task oriented physiotherapy on gross motor function, balance and gait in children with spastic cerebral palsy.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: Qamar Mahmood, PhD
- Telefonnummer: 03335151063
- E-mail: Qamar.mehmood@riphah.edu.pk
Studiesteder
-
-
Fedral
-
Islamabad, Fedral, Pakistan, 44000
- National Institute of Rehabilitation Medicine
-
Kontakt:
- Qamar Mahmood, PhD
- Telefonnummer: 03335151063
- E-mail: Qamar.mehmood@riphah.edu.pk
-
Kontakt:
- Mahnoor Baloch, MSPPT*
- Telefonnummer: 03185695550
- E-mail: mahnoorbaloch1191@gmail.com
-
Ledende efterforsker:
- Mahnoor Baloch, MSPPT*
-
Islamabad, Fedral, Pakistan, 44000
- Pakistan Institute of Medical Sciences
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Children diagnosed with spastic cerebral palsy.
- Age between 5-12 years.
- Gross Motor Function Classification System (GMFCS) levels I-III.
- Ability to follow simple verbal commands.
- Medically stable condition.
- Ability to maintain sitting or standing with minimal assistance.
- Have parental/guardian consent for participation
Exclusion Criteria:
- Severe visual or hearing impairments.
- Orthopedic surgery within the previous 6 months.
- Botulinum toxin injection within the previous 6 months.
- Uncontrolled seizures or severe cognitive impairment.
- Other neurological or musculoskeletal disorders affecting mobility.
- Severe fixed deformities limiting participation.
- Have severe cognitive impairment preventing participation
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Conventional Physiotherapy
|
Participants in the control group will receive conventional physiotherapy for a duration of 6 weeks. The treatment will be administered three times per week, with each session lasting approximately 45 minutes |
|
Eksperimentel: Video-Based Visual Feedback + Task-Oriented Physiotherapy
|
Participants in the experimental group will receive video-based visual feedback combined with task-oriented physiotherapy for a period of 6 weeks. The intervention will be administered three times per week, with each session lasting approximately 45 minutes |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Gross Motor Function Measure
Tidsramme: 6 weeks
|
A standardized tool used to assess gross motor abilities in children with cerebral palsy. It measures activities such as sitting, crawling, standing, and walking. Scores range from 0-100, with higher scores indicating better motor function |
6 weeks
|
|
Pediatric Balance Scale
Tidsramme: 6 weeks
|
A balance assessment tool designed for children. It evaluates a child's ability to maintain balance during everyday activities such as standing, reaching, turning, and stepping. The Pediatric Balance Scale (PBS) has a maximum total score of 56 points (14 items × 4 points each). Higher scores indicate better balance performance. |
6 weeks
|
|
Observational Gait Scale (OGS)
Tidsramme: 6 weeks
|
A simple observational tool used to assess walking patterns in children with cerebral palsy. It evaluates different aspects of gait, such as foot placement, knee movement, and overall walking quality. The Observational Gait Scale (OGS) has a maximum total score of 22 points (6 items scored from 0-3 and 1 item scored from 0-4). Higher scores indicate a more normal gait pattern. |
6 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Qamar Mahmood, Riphah International University
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- REC/MS-PT/02581 Mahnoor
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .