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Recruiting NCT07714031

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

No phase Interventional Wrist Joint Overuse Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: 3- dimensional Articular fascial release approach, 3 Dimensional soft tissue release approach.
Who it may be relevant to
Registry conditions: Wrist Joint Overuse Syndrome. Basic parameters: 20 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Interventions

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

Primary outcome measures

  • Pain Intensity [Time frame: 3 weeks]
  • Range of Motion [Time frame: 3 weeks]
Secondary outcome measures (1)
  • Functional disability [Time frame: 3 weeks]

Eligibility criteria

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

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Dr Rubina Zulfqar — Faisalabad

Identifiers

NCT: NCT07714031 · TUF/EIRB/177/26

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗