CClinicalTrials.gg
RecruitingNCT07714031Updated Jul 23, 2026

Comparative Effects of 3-Dimensional Articular and Soft Tissue Myofascial Release Approach in Patients With Overuse Syndrome of Wrist Joint

An interventional study of 3- dimensional Articular fascial release approach and 3 Dimensional soft tissue release approach in Wrist Joint Overuse Syndrome, sponsored by University of Faisalabad. Recruiting at 1 site in Pakistan. Open to participants aged 20 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-07-23.

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

Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Randomized
Ages
20 Years to 50 Years
Sex
All
01

Study summary

Overuse syndrome or RSI is challenging condition among clinicians now a days. These are MSK disorders which are related to bones, muscles and tendons peripheral nerve entrapment and vascular changes. These MSK disorders commonly effects back, neck and upper limbs although it least effect lower limbs. These problems occur from repetitive movements, ergonomic hazards, awkward postures and work related problems. This study aims to assess the comparative effects of 3 dimensional articular myofascial release approach and soft tissue myofascial release approach in patients with overuse syndrome of wrist joint. A randomized controlled trial will be conducted age between 20-55 years, both male and female genders will be included diagnosed with overuse syndrome of wrist. Diagnosis will be made on the basis of diagnostic criteria which will include tenderness present in intrinsic muscles and pain in radial ligament of wrist. Participants will be chosen through consecutive sampling.

Each participant will sign a consent form before taking part in the study. According to sample size 46 participants will be divided into two groups. Each group will include 23 participants which will be divided through lottery method. Both groups will receive baseline treatment which will include hot-pack for 15 minutes. Group a will be treated with articular fascial release and group b will be treated with soft tissue release for 3 sessions per week, for 3 weeks. After therapy session both groups will perform wrist rom exercises including wrist flexion, extension, radial and ulnar deviation 5 repetitions each. Outcome measuring tools will be numeric pain rating scale (NPRS) for pain, disabilities of arm, shoulder and hand (DASH) for functional disability, patient rated wrist evaluation (PRWE) specifically wrist functions evaluation and goniometer for range of motion. Data will be investigated through SPSS.

02

Conditions studied

  • Wrist Joint Overuse Syndrome
03

Who can participate

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

Inclusion criteria

  • Patients between 20-55 years of age

    • Male and female
    • Participants involved in repetitive movements of hands e.g computer workers ( 2026/3/4
    • Patients who have gradual onset of pain not sudden
    • Reproduction of pain with wrist flexion, extension, ulnar and radial deviation
    • Patients with >10% reduced ROM of wrist joint as compared to contralateral side
    • Participants who will willing to participate

Exclusion criteria

Exclusion Criteria:

Specific disease of wrist e.g RA, gout, infection

  • Patients with traumatic wrist pathology (such as scaphoid fracture, distal radius fracture)
  • Neuropathic compromise patients such as diabetic neuropathy, CTS
  • Open wound
  • Suspected or confirmed malignancy in wrist joint
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
46 participants (estimated)

Study arms

  • Experimental
    3- dimensional Articular fascial release approach

    Procedure: 3- dimensional Articular fascial release approach

  • Experimental
    3 Dimensional soft tissue release approach

    Procedure: 3 Dimensional soft tissue release approach

Interventions

  • Procedure3- dimensional Articular fascial release approach

    Hot pack for 15 mins.3- dimensional Articular fascial release approach

  • Procedure3 Dimensional soft tissue release approach

    Hot pack for 15 mins. 3 Dimensional soft tissue release approach * Technique: Apply gentle sustained pressure in all three planes. Hold 30-90 seconds while sensing tissue give hold until all the symptoms and fascial release feel. Encourage slow diaphragmatic breathing exhalation facilitates release. 4. Avoid: Pressure on bony surfaces and nerve trunks area 5. Dose and frequency * Per site 8-12 minutes of fulcrum work (including holds and plane cycles) * Session: 20-40 minutes total including warm up, 1-3 fulcrum site integration and education 6\. Frequency: Total 3 weeks, per week 3 sessions, total sessions 7. After treatment will include ROM exercises including wrist flexion, extension, radial deviation and ulnar devi

05

What researchers measure

Primary outcomes

  1. Pain Intensity

    Pain Intensity will be measured by using the Numeric Pain Rating Scale, the patients rate their pain on a scale from 0 (no pain) to 10 (worst possible pain).NPRS scale consists of 11 points in which 0 is no pain while 10 is worst pain.

    Time frame: 3 weeks

  2. Range of Motion

    Range of Motion will be measured by using Goniometry the improvement in ROM shows good results.

    Time frame: 3 weeks

Secondary outcomes

  1. Functional disability

    Functional disability will be measured by using The Disabilities of Arm, Shoulder and Hand (DASH) and Patient-rated wrist evaluation form (PRWE). The DASH questionnaire is consists of thirty items which asses the physical function and symptoms. It involve five options for response of each item. Ultimate score is calculated through the formula below: DASH score = {(sum of n responses)-1}\*25, n=number of complete responses, the highest score showed improvement. While The PRWE is a self administrated questionnaire which is patient specific which consist of 15 items. It was designed for measurement of activities of daily living of wrist pain and disability and consist of 2 subscales; pain and function.A score of 100 represent the worst functional score while the score 0 indicate no disability.

    Time frame: 3 weeks

06

Study locations

1 of 1 sites recruiting
  • Dr Rubina Zulfqar
    Faisalabad, Punjab Province 38000, Pakistan
    Recruiting
07

Registry details

Key details

Study ID
NCT07714031
Lead sponsor
University of Faisalabad
Responsible party
Rubina Zulfqar (Assistant Professor, University of Faisalabad) — Principal investigator
First posted
Jul 20, 2026
Start date
Jul 14, 2026 (estimated)
Primary completion
Aug 9, 2026 (estimated)
Completion
Aug 9, 2026 (estimated)
Last update
Jul 23, 2026

Study contacts

Dr Rubina Zulfqar
Contact
drrubinazulfqar355@gmail.com
+923414291664

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion