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Virtual Reality Combined With Active Mobilization Post Flexor Tendon Repair

Virtual Reality Combined With Controlled Early Active Mobilization Post Flexor Tendon Surgical Repair

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07875452
Enrollment
54
Registered
2026-10-15
Start date
2026-05-12
Completion date
2028-04-01
Last updated
2026-10-15

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

Conditions

Flexor Tendon Injury

Brief summary

The purpose of this study is to evaluate the efficacy of combining IVR-based rehabilitation with a controlled early active mobilization protocol on functional outcomes, digit range of motion, grip strength, pinch strength and pain following flexor tendon repair.

Interventions

controlled early active mobilization

COMBINATION_PRODUCTactive mobilization plus IVR-based rehabilitation.

controlled early active mobilization protocol plus IVR-based rehabilitation.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing hand flexor tendon repair (within 24 hours up to 10 days) from both sexes. * Age ranges from 18 to 50 years * Only patients with isolated injuries to the flexor digitorum profundus and/or superficialis tendons will be selected * Ability to follow instructions and participate in rehabilitation sessions

Exclusion criteria

* Patients with associated injuries (fractures, skin loss, crush injury, thumb flexor tendon injuries, nerve injuries and vascular injuries) or systemic conditions (rheumatoid arthritis and diabetes) will be excluded * Previous trauma or surgery to the affected hand. * Cognitive impairments interfere with participation . * Participation in other rehabilitation programs. * Bilateral hand injuries * Delayed surgery after injury.

Design outcomes

Primary

MeasureTime frame
pinch strength(pinch gauge kg)8 weeks and 12 weeks after surgery

Countries

Egypt

Contacts

CONTACTWarda Ali
awarda560@gmail.com01018045663

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Oct 16, 2026