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Effect of constraint-induced movement therapy on hand function of patients with median and ulnar nerve injury

Efficacy of occupation-based interventions versus exercise therapy in constraint-induced movement therapy on upper limb function after median and ulnar nerve repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016011710806N4
Enrollment
30
Registered
2016-04-22
Start date
2016-03-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Median and Ulnar Nerve Injury. Other lesions of median nerve, Lesion of ulnar nerve

Interventions

Intervention 1: Occupation-based constraint-induced movement therapy group: immobilization of healthy hand for 6 hours each day 4 weeks. occupation-based interventions for 3 hours a day, 3 days a wee
Rehabilitation
Occupation-based constraint-induced movement therapy group: immobilization of healthy hand for 6 hours each day 4 weeks. occupation-based interventions for 3 hours a day, 3 days a week, during 4 week
Exercise therapy based constraint-induced movement therapy group: immobilization of healthy hand for 6 hours each day 4 weeks. Exercise-based interventions for 3 hours a day, 3 days a week, during 4 w
control group: 1.5 hours of practice each day by own patient alone in his/her home without therapist for 4 weeks

Sponsors

Research Deputy of Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: chronic condition (at least 6 months after nerve repair); Non-use learning in injured limb (score less than 2.5 in Motor Activity Log); lack of any non-healed fractures or tendon ruptures; score less than 10 in Beck depression questionnaire; Lack of neurologic disorders related to the central nervous system; Age between 18-55 years Exclusion criteria: any surgery during the study period; complex regional pain syndrome; No participation in more than 2 intervention sessions

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sensation of fingers. Timepoint: before, after, and 1 month afterthe intervention ending. Method of measurement: touch perception at volar side of the pulp of index finger (median nerve) and littile finger (ulnar nerve) by semmes-weinstein monofilaments.;Occupational performance. Timepoint: before, after, and 1 month afterthe intervention ending. Method of measurement: patients own score to the performance and satisfaction of performance in preferred occupations in a 0-10 scale in COPM Questionnaire.;Disability rate of upper limb. Timepoint: before, after, and 1 month afterthe intervention ending. Method of measurement: patients own score to 30 questions of DASH questionnaire in a 1-5 likert scale.;Hand dexterity. Timepoint: before, after, and 1 month afterthe intervention ending. Method of measurement: number of transfered cubes in one minutes in Box and Block test.

Secondary

MeasureTime frame
Motivation. Timepoint: before, after, and 1 month afterthe intervention ending. Method of measurement: This scale is a visual scale. patient chooses one of the pictures that is according to his/her view about Dominancy, Valence, and arousal.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMalahat Akbarfahimi

Iran Univertsity of Medical Sciences

akbarfahimi.m@iums.ac.ir+98 21 2222 8052

Outcome results

None listed

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