Controlled Active Motion vs Early Passive Mobilization for Flexor Tendons Repair

N/ARecruitingNCT06420648

University of Hail50 enrolled

Overview

a randomized controlled trial tends to compare 2 rehabilitation approaches - early passive mobilization (EPM) and controlled active motion (CAM) - that are commonly used in the treatment of post-surgical flexor tendon repair of the hand

a randomized controlled trial tends to compare 2 rehabilitation approaches commonly used in the treatment of post-surgical flexor tendon repair of the hand. in this study, the authors try to fill the gap in the literature regarding the more effective approach. the comparisons between both approaches were scarce in previous literature. Participants will be randomly allocated to one of two treatment groups: early passive mobilization (EPM) using a modified Kleinert protocol or controlled active motion (CAM) using a modified Duran technique (n=20). Patients were assessed at baseline and then at the 6th and 12th weeks of interventions to quantify total active motion (TAM) of the proximal and distal interphalangeal joints using goniometry, and grip strength with dynamometry. the disability level will be assessed using the Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

Conditions

Flexor Tendon Rupture

Interventions

Early passive mobilizationOTHER

a rehabilitation protocol for post-surgical repair of flexor tendons of the hand

Controlled active motionOTHER

a rehabilitation protocol for post-surgical repair of flexor tendons of the hand

Eligibility

Sex: ALLMin age: 25 YearsMax age: 50 Years

Medical Language ↔ Plain English

Inclusion Criteria: * males or females * between 25-50 years * Post-surgical repair of the flexor digitorum profundus (FDP) and superficialis (FDS) tendons of a single-digit * the case should be recent (2-3 days post-surgical) Exclusion Criteria: * age below 25 or above 50 * a systemic disease affecting hand joints such as rheumatic arthritis * thumb flexor tendon repair will be excluded * chronic cases * concurrent injuries such as phalangeal fractures, joint injuries, or significant skin loss

Locations (2)

Hail University Poly Clinic

Hail, Saudi Arabia

RECRUITING

Hisham Hussein

Hail, Saudi Arabia

RECRUITING

Outcomes

Primary Outcomes

Total active motion (TAM)

Active range of motion in proximal interphalangeal joint (PIP) and the distal interphalangeal joint (DIP) of the injured digits will be measured by manual hand goniometry. Outcome will be expressed by Strickland formula. TAM (%) = (Active flexion of PIP+DIP) - Extension Lag of both joints/175× 100 This formula can determine the percentage of recovery of TAM. The results of TAM (%) are classified in four categories: "Excellent, good, fair, and poor"

Time frame: at baseline

Total active motion (TAM)

This formula can determine the percentage of recovery of TAM. The results of TAM (%) are classified in four categories: "Excellent, good, fair, and poor" This formula determined the percentage of recovery of TAM. The results of TAM (%) were classified in four categories: "Excellent, good, fair, and poor"

Time frame: after the 12th week of intervention

handgrip strength

Hand dynamometer (Jammer dynamometer) will be used to evaluate hand grip strength. Measurements will be taken for both hands for three times. The mean of three trials will be taken for every measurement occasion. The mean value in the injured hand will be expressed as percentage of the mean value in the non-injured hand as follows: % of hand grip strength = Mean grip strength in the involved hand/ Mean grip strength in the uninvolved hand × 100.

Time frame: baseline

handgrip strength

Time frame: after the 12th week of intervention

Functional disability

The Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire will be used to measure the functional disabilities. It is a valid questionnaire used in a number of other disabling conditions of the hand. A DASH-questionnaire score, ranges from 0 to 100. A score of 0 means no difficulties in daily living and a score of 100 means maximum difficulties in performing tasks of daily living

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.