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Mirror Therapy and Hand Rehabilitation

Mirror Therapy in Patients With Hand Orthopedic Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01503762
Enrollment
23
Registered
2012-01-04
Start date
2009-01-31
Completion date
2011-12-31
Last updated
2012-02-28

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

Conditions

Hand Fractures

Keywords

Hand Flexor tendon Injuries, hand Extensor Tendon Injuries, Hand Joint Dislocations and subluxation

Brief summary

Objective: The purpose of this study is to determine effects of mirror therapy in restoring hand function in patients with flexor lag following orthopedic injuries. Methods: In a prospective randomized controlled trial, 22 patients with Flexor Lag will be measured. Intervention group will receive mirror therapy, 30-minute a day, 5 days a week for 3-week, as well, half an hour conventional rehabilitation after each mirror therapy session. Patients in the control group will receive the same treatment program, but instead of mirror, they will directly observe the affected hand. Outcome measures including Total Active Motion (TAM), and Disabilities of Arm, Shoulder and Hand (DASH) questionnaire will be administered before and after the treatment period and 3 weeks after the final treatment session.

Interventions

OTHERMirror therapy

mirror therapy

OTHERClassical rehabilitation techniques

splinting, tendon gliding, active range of motion, activities of daliy living

Sponsors

Ahvaz Jundishapur University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* hand orthopedic Injuries * more active range of motion than passive range of motion

Exclusion criteria

* crush injuries * hand deformities * not treated fractures and tendon ruptures * complex regional pain syndrome * psychiatric problems

Design outcomes

Primary

MeasureTime frameDescription
Total Active Motion6 WeeksSum of Range of Motion in Metacarpophalangeal, Proximal Interphalangeal and Distal Interphalangeal Joints.

Secondary

MeasureTime frame
Disabilities of the Shoulder, Arm, hand6 Weeks

Countries

Iran

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026