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Effectiveness of Occupation-Based Exercise Program in Zone 2 Flexor Tendon Injuries

Effectiveness of Occupation-Based Exercise Program Added to Conventional Rehabilitation Program on Hand Functions, Range of Motion, Grip Strength, Pain and Kinesiophobia in Zone 2 Flexor Tendon Injuries

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07046416
Enrollment
65
Registered
2025-07-01
Start date
2025-07-31
Completion date
2025-12-31
Last updated
2025-07-09

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

Conditions

Tendon Injuries, Zone 2 Flexor Tendon Lacerations of the Hand

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.

Interventions

OTHEROccupation-Based Exercise Program

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.

OTHERConventional therapy 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.

Sponsors

Istanbul University
CollaboratorOTHER
Berat Güngör
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Disabilities of The Arm, Shoulder and Hand Questionnaire (DASH)Participants will be evaluated at 6th, 10th and 16th weeks postoperative.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).

Secondary

MeasureTime frameDescription
Modified Strickland ClassificationParticipants will be evaluated at 6th, 10th and 16th weeks postoperatively.Range of motion of the fingers will be measured with a goniometer and results will classified according to Modified Strickland Classification
Numerical Pain Rating Scale (NPRS)Participants will be evaluated at 6th, 10th and 16th weeks postoperatively.The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. Higher scores indicating greater pain intensity.
Tampa Kinesiophobia ScaleParticipants will be evaluated at 6th, 10th and 16th weeks postoperativelyThe scale total scores range from 17 to 68 where the lowest 17 means no or negligible kinesiophobia, and the higher scores indicate an increasing degree of kinesiophobia.
Grip strentghParticipants will be evaluated at 6th, 10th and 16th weeks postoperatively.Hand grip strength will be measured with a hand dynamometer and finger grip strength with a pinchmeter.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026