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A comparison study of video-based and physician-guided exercise for post-operative rehabilitation after distal radius fracture: A randomized controlled trial

A comparison study of video-based and physician-guided exercise for post-operative rehabilitation after distal radius fracture: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251229021
Enrollment
26
Registered
2025-12-29
Start date
2025-06-09
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients with distal radius fractures treated with volar locking plate fixation Radius fractures Rehabilitation Exercise Therapy Randomized controlled trial

Interventions

Participants in this group receive a self-directed home exercise program via a unique QR code linked to an instructional video hosted on a secure cloud platform (Google Drive). A physiatrist provided
Experimental Other,No Intervention Other
Video-based exercise,Physician-guided exercise

Sponsors

Maharat Nakhon Ratchasima Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with displaced intra-articular distal radius fracture who have undergone surgical management via volar locking plate fixation. 2. Aged between 18 and 75 years. 3. Newly diagnosed distal radius fracture. 4. Ability to effectively communicate in the Thai language. 5. Ability to access and utilize video-based media via a smartphone or other compatible digital devices, either by the patient or their primary caregiver. 6. Willingness to participate in the study and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who received additional fixation methods alongside the locking volar plate, such as K-wire fixation. 2. Patients with co-existing injuries or inflammatory conditions (e.g., arthritis) or peripheral nerve injuries affecting the ipsilateral upper extremity. 3. Patients with a history of Stroke, Traumatic Brain Injury (TBI), or Spinal Cord Injury (SCI) resulting in motor deficits or weakness in the affected upper limb. 4. Patients requiring or requesting continuous, supervised physical therapy sessions conducted by a therapist. 5. Patients with cognitive impairments or communication disorders that impede their ability to understand, learn, or adhere to the exercise instructions.

Design outcomes

Primary

MeasureTime frame
Thai version of the Patient-Rated Wrist Evaluation score at 2 weeks, 6-8 weeks and 12-14 weeks post-surgery Patient reported outcome using Th-PRWE questionnaire

Secondary

MeasureTime frame
Wrist range of motion at 2 weeks, 6-8 weeks and 12-14 weeks post-surgery Using a standard goniometer,Handgrip strength at 2 weeks, 6-8 weeks and 12-14 weeks post-surgery Measured in kilograms using a calibrated hand dynamometer,Knowledge Assessment Score at 2 weeks, 6-8 weeks and 12-14 weeks post-surgery Using a custom-developed questionnaire

Countries

Thailand

Contacts

Public ContactThitiwad Rueangsaowapong

Department of Rehabilitation Medicine

thitiwad.kr@cpird.in.th0828598957

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026