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To determine the combined effects of trans-cranial direct current stimulation and mirror therapy on neuromuscular development and mental health in children with spastic quadriplegic cerebral palsy.

Effects of trans-cranial direct current stimulation with and without mirror therapy on neuromuscular development and mental health in children with spastic quadriplegic cerebral palsy

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231227060542N1
Enrollment
105
Registered
2024-01-26
Start date
2024-01-08
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Cerebral Palsy. Spastic quadriplegic cerebral palsy

Interventions

Intervention 1: Subjects will be evaluated for eligibility before allocation to one of three groups: Group-A (TDCS, MT with routine Physical Therapy), Group-B (TDCS with routine Physical Therapy) and

Sponsors

nil
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 7 Years

Inclusion criteria

Inclusion criteria: Diagnosed patients of spastic quadriplegic cerebral palsy via physical examination aged from 3-7 years from both genders , Level-I and II patients on the Gross Motor Function Classification System (GMFCS) who can walk with or without assistance, respectively , Tone less than or equal to 2 on the modified Ashworth scale Having good understanding for the commands

Exclusion criteria

Exclusion criteria: Athetoid cerebral palsy, ataxic an mixed variety will be excluded• Monoplegia, diplegic hemiplegic cerebral palsy patients will be excluded• History of any neurosurgery or neurolytic block (botulinum toxin and phenol) in the previous 6 months or any cancerous history or orthopedic deformity Any integumentary condition, seizure history or metal implant especially in the skull or use of hearing aids

Design outcomes

Primary

MeasureTime frame
Motor development, Motor control, muscle performance, anthropometry, mental health. Timepoint: Before treatment, after two weeks and after 10 weeks. Method of measurement: Shoaib motor development tool, Fugal Mayer, isokinetic Dynamometer, Tape, stadiometer and weight machine, SDQ questionnaire.

Secondary

MeasureTime frame
Quality of life. Timepoint: before treatment, after 6months. Method of measurement: SF-36.

Countries

Pakistan

Contacts

Public ContactAshfaq Ahmad

The University of Lahore

ashfaq.ahmad@uipt.uol.edu.pk+92 300 9449192

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 5, 2026