Skip to content

Effect of Leap Motion Tracking Device on Pain, Range of Motion, Muscle Strength And Functional Parameters in patients with Distal Radial Fracture

Efficacy of Leap Motion Tracking Device versus Conventional Rehabilitation on Pain, Range of Motion, Muscle Strength and Functional Parameters in patients with Distal Radial Fracture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033498
Enrollment
40
Registered
2021-05-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: S62- Fracture at wrist and hand level

Interventions

Intervention1: Leap Motion Controller Device: 5 games, each game concentrating on the specific wrist movement, for 5 minutes each, for 30 minutes of the treatment session. Control Intervention1: Conve

Sponsors

Datta Meghe Institute of Medical Sciences Ravi Nair Physiotherapy College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients must be diagnosed with an A3 extraarticular multi-fragmentary distal radial fracture type and treated conservatively with plaster cast immobilization and closed reduction. 2. Participants must accept and sign the Informed consent. 3. No previous history of wrist/ hand fracture, history of inflammatory arthritis, or any possible upper limb fracture. 4. Patients who are able to comprehend

Exclusion criteria

Exclusion criteria: 1. Participants who were treated for DRF reduction and/or fixation with some form of surgical intervention (e.g. external fixation, volar plate, and Kirschner wires). 2. Patients with Mini-Mental score less than 26 points on the examination. 3. After the removal of the immobilization, patients with immediate complications like malunion or non-union. 4. Patients with past trauma either in arms or hands that had impaired function. 5. Patients with inflammatory or non-inflammatory diseases and neurological disorder were excluded.

Design outcomes

Primary

MeasureTime frame
1. Disabilities of the Arm, Shoulder and Hand Outcome Questionnaire (DASH) 2. Universal GoniometerTimepoint: 1. Disabilities of the Arm, Shoulder and Hand Outcome Questionnaire (DASH) 2. Universal Goniometer

Secondary

MeasureTime frame
1. Visual Analogue Scale (VAS) 2. Grip Strength using Hand DynamometerTimepoint: Pre Treatment day 1 Post Treatment 6 weeks

Countries

India

Contacts

Public ContactDr Waqar M Naqvi

Ravi Nair Physiotherapy College

waqar.naqvi@dmimsu.edu.in9021699000

Outcome results

None listed

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