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RecruitingNCT06420648Updated Jun 6, 2024

Controlled Active Motion vs Early Passive Mobilization for Flexor Tendons Repair

An interventional study of Early passive mobilization and Controlled active motion in Flexor Tendon Rupture, sponsored by University of Hail. Recruiting at 2 sites in Saudi Arabia. Open to participants aged 25 Years to 50 Years. Per ClinicalTrials.gov, last updated 2024-06-06.

Sponsored by University of Hail · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Oct 2024, 1 year 11 months ago, but the record still lists the study as recruiting.
  • Started Jun 2024; still recruiting 2 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
25 Years to 50 Years
Sex
All
01

Study summary

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

Read the detailed description

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.

02

Conditions studied

  • Flexor Tendon Rupture

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03

In context

Rupture

557 studies on the registry are indexed under Rupture; 97 are open to participants now.

This study's planned enrollment of 50 is below the median of 72 across 334 interventional studies indexed under Rupture.

Browse Rupture studies →

Lead sponsor

University of Hail is the lead sponsor of 23 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Early passive mobilization group

    The modified Kleinert protocol will be used as an EPM procedure. Within 3 to 5 days following surgery, the affected hand will be placed inside the dorsal slab Kleinert splint with the wrist in 30-40 flexion; metacarpophalangeal joint (MP) in 60-70-degree flexion; PIP and DIP joints in extension. Rubber band traction will be directed to the fingernail from the wrist, with a palmar pulley system. All patients will perform passive flexion and active extension exercises with an active hold for 2-3 seconds 10 times per hour. Traction will be removed at the end of 3rd week and very gentle active flexion will start at the 4th week. The splint will be removed in the 5th-6th weeks. Blocking exercises will be started at 7th-8th weeks and resisted exercises will be started after the 8th week with the full function permitted by week 12th week .

    Other: Early passive mobilization

  • Experimental
    Controlled active motion group

    A modified CAM protocol will be used. Exercises will be performed hourly for 10 repetitions in the form of passive flexion and active extension exercises with an active hold of the fingers in the flexed position for 2-3 seconds.

    Other: Controlled active motion

Interventions

  • OtherEarly passive mobilization

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

    Also known as: modified Kleinert protocol

  • OtherControlled active motion

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

06

What researchers measure

Primary outcomes

  1. 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

  2. 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

  3. 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

  4. 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: after the 12th week of intervention

  5. 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

    Time frame: at baseline

  6. 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

    Time frame: after the 12th week of intervention

07

Study locations

2 of 2 sites recruiting
  • Hail University Poly Clinic
    Hail, 2442, Saudi Arabia
    Recruiting
  • Hisham Hussein
    Hail, 3994, Saudi Arabia
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — data will be available with the senior author upon request

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 6, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06420648
Lead sponsor
University of Hail
Responsible party
Hisham Mohamed Hussein (principal investigator, University of Hail) — Principal investigator
First posted
May 20, 2024
Start date
Jun 4, 2024
Primary completion
Oct 30, 2024 (estimated)
Completion
Dec 30, 2024 (estimated)
Last update
Jun 6, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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