NCT07046416

Brief Summary

Aim of the study is to evaluate the effects of a 4-week occupation-based exercise program given in addition to the conventional rehabilitation program on hand functions, range of motion, grip strength, pain and kinesiophobia in the post-operative rehabilitation of patients aged 18-65 years with zone 2 flexor tendon repair. Expected results: To prove the effectiveness of occupation-based exercises in order to reduce the failure rates seen in the rehabilitation of zone 2 flexor tendon injuries, to increase patient compliance and motivation during the rehabilitation process, to improve functional outcomes by ensuring its inclusion in conventional treatment and to increase patient satisfaction.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
65

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 23, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 1, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

July 1, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

July 9, 2025

Status Verified

July 1, 2025

Enrollment Period

4 months

First QC Date

June 23, 2025

Last Update Submit

July 4, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Disabilities of The Arm, Shoulder and Hand Questionnaire (DASH)

    In DASH Questionnaire a higher scores indicate a greater level of disability and severity, whereas, lower scores indicate a lower level of disability. The score on both test ranges from 0 (no disability) to 100 (most severe disability).

    Participants will be evaluated at 6th, 10th and 16th weeks postoperative.

Secondary Outcomes (4)

  • Modified Strickland Classification

    Participants will be evaluated at 6th, 10th and 16th weeks postoperatively.

  • Numerical Pain Rating Scale (NPRS)

    Participants will be evaluated at 6th, 10th and 16th weeks postoperatively.

  • Tampa Kinesiophobia Scale

    Participants will be evaluated at 6th, 10th and 16th weeks postoperatively

  • Grip strentgh

    Participants will be evaluated at 6th, 10th and 16th weeks postoperatively.

Study Arms (2)

Occupation-based exercise group

EXPERIMENTAL
Other: Occupation-Based Exercise Program

Conventional therapy group

ACTIVE COMPARATOR
Other: Conventional therapy group

Interventions

In the occupation-based exercise program, while trying to improve the range of motion and muscle strength of the hand, it is aimed to successfully return to daily life activities. For this reason daily activities are used instead of memorized range movements. In this way, the occupation-based exercise program provides a physical recovery in patients with hand injuries, while providing positive improvements in parameters related to the mind and spirit. Patients' participation, motivation and compliance with the treatment are increased in the hand rehabilitation process, which can be challenging for patients. In addition to the conventional treatment program, the study/experimental group, will be given occupation-based exercises for a total of 4 weeks between the 6th and 10th weeks postoperatively, 2 days a week with a physiotherapist and the other days with a home program.

Occupation-based exercise group

Conventional group treatment will be according the early passive hand rehabilitation program. Conventional group will be followed with a cast-splint made by the surgical team for the first 4 weeks within the scope of the conventional treatment program. From the 4th week onwards, the duration of splint use is gradually reduced and is completely discontinued from the 6th week onwards. At the end of the 4th week, depending on the wound condition, contrast bath, scar massage, retrograde massage, active and passive flexion, active extension and tendon shifting exercises are applied as tolerated. After the 6th week, isolated block exercises and stretching exercises are added if there is contracture. Strengthening exercises are started from the 8th-10th week.

Conventional therapy group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Between the ages of 18-65
  • Flexor zone 2 injury
  • At least 1 flexor digitorum superfisialis or flexor digitorum profundus tendon repair
  • No visual and hearing impairment
  • Have the cognitive function to coordinate and carry out simple commands

You may not qualify if:

  • Concomitant flexor pollicis longus tendon injury
  • Concomitant extensor tendon injury
  • Accompanying fracture
  • Associated median/ulnar/radial nerve injury
  • Less than 50% partial flexor tendon injury
  • Cognitive impairment resulting in an inability to understand and carry out simple commands
  • Not being able to comply with the rehabilitation protocol to be applied after surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul Unıversity, Istanbul Faculty of Medicine, Department of Physical Medicine and Rehabilitation

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Tendon Injuries

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Dr.

Study Record Dates

First Submitted

June 23, 2025

First Posted

July 1, 2025

Study Start

July 1, 2025

Primary Completion

November 1, 2025

Study Completion

December 1, 2025

Last Updated

July 9, 2025

Record last verified: 2025-07

Locations