Skip to content

Effect of Modified Hand Therapy (Constraint-Induced Movement Therapy) Compared to Robot-Assisted Therapy on Hand Function and Daily Life in Children with Cerebral Palsy Affecting One Side of the Body

Effect of Modified Constraint Induced Movement Therapy in Comparison with Robotic Assisted Therapy on Hand Function and Quality of Life in Hemiplegic Cerebral Palsy Children - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081316
Enrollment
36
Registered
2025-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G819- Hemiplegia, unspecified

Interventions

Intervention1: Modified Constraint-Induced Movement Therapy Group A: Modified Constraint-Induced Movement Therapy (mCIMT) is an intervention used to improve function and mobility in the more affected
Reaching forward to hold a glass and drinking from it, Picking up a comb and combing hair, Turning on and off a light switch, Writing with a pen, Moving the pegs each task last for 2 minutes. Control
picking a pen, moving pegs etc, it s well fitted and aligned with regular conventional therapy, treatment lasting for 30-minute session, each task last for 2 minutes per day for 8weeks.

Sponsors

Self
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Informed consent from those whose parents/ward legally authorized guardian willing to allow their child to participate as volunteers are included in study. Diagnosed with Hemiplegic Cerebral palsy. Age group: 9-16 yr. old Modified Ashworth scale (MAS) less than grade 3 Manual Ability Classification System level I-IV Modified Mini mental state Examination score more than 20

Exclusion criteria

Exclusion criteria: History of Epilepsy Presence of Behavioral problem Orthopedic surgeries Botulinum surgeries (Any medical intervention within 6 months including) Ventriculoperitoneal shunt or implant devices

Design outcomes

Primary

MeasureTime frame
1. Modified Ashworth Scale 2. QUEST 3. The Fugl Meyer Assessment (FMA) Timepoint: Pre Intervention (0WEEKS) Post Intervention (6weeks)

Secondary

MeasureTime frame
1. The Fugl Meyer Assessment (FMA) Timepoint: Pre Intervention (0WEEKS) Post Intervention (6weeks)

Countries

India

Contacts

Public ContactDr Satya Guruprasad

dayananda sagar university - college of physiotherapy

ppl-physio@dsu.edu.in9167986403

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026