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Clinical Trials/CTRI/2026/01/102339
CTRI/2026/01/102339Not yet recruitingPhase 2/3

Effectiveness Of Autogenic Biofeedback Combined With Hand Rehabilitation Activities On Upper Limb Function Among Patients With Colles Fracture

LOKESWARAN K1 site in 1 country30 target enrollmentStarted: February 3, 2026Last updated:

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1

Study Overview

Brief Summary

Before enrolling each participant in the study, informed consent will be obtained from  their participant , using consent forms approved by the Institutional Review Board of Chettinad University Hospital (CHRI, CARE). A total of 30 individuals, aged 18 to 60 years and diagnosed with colles fracture will be recruited from the Occupational Therapy And Orthopaedic Department at Chettinad Hospital and Clinics in the Chengalpattu District. After obtaining consent and confirming inclusion criteria, participants will be randomly assigned into two groups: an intervention group is 15  and a control group is 15. Pre-intervention assessment of the independency will be conducted using the Disability Of Arm Shoulder And Hand (DASH).The experimental group will receive Autogenic Biofeedback Combined With Hand Rehabilitation Activities , while the Control Group will not receive any intervention by researcher during this time. Eg: Each session will last 30 minutes, 5 days per week, for 4 weeks. After theweeks intervention period, the independency will be reassessed using the same tools Disability Of Arm Shoulder And Hand (DASH). Pre  and post-intervention scores will be statistically analysed to evaluate the effectiveness of the intervention.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Age group around 18 to 60 Both male and female Diagnosed with unilateral colles fracture, Patient is in early mobilization or post cast removal phase around 4 to 6weeks with fracture radiologically stable, No severe visual impairment No serious cognitive impairment, No severe pain more than 5 in NPRS scale.

Exclusion Criteria

  • Unstable fracture or incomplete bone healing, severe pain or swelling that limits active movement,open wound ,infection or post surgical complications in the affected limb, assoiciated nerve injury causing severe motor or sensory loss, multiple fracture or bilateral upper limb injuries.

Investigators

Sponsor
LOKESWARAN K
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr B NIBEDITA PRIYADARSHINEE

Chettinad academy of research and education

Study Sites (1)

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