Comparative Effects of 3-Dimensional Articular and Soft Tissue Myofascial Release Approach in Patients With Overuse Syndrome of Wrist Joint
1 other identifier
interventional
46
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 9, 2026
CompletedStudy Start
First participant enrolled
July 14, 2026
CompletedFirst Posted
Study publicly available on registry
July 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 9, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 9, 2026
CompletedJuly 23, 2026
July 1, 2026
26 days
June 9, 2026
July 22, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
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.
3 weeks
Range of Motion
Range of Motion will be measured by using Goniometry the improvement in ROM shows good results.
3 weeks
Secondary Outcomes (1)
Functional disability
3 weeks
Study Arms (2)
3- dimensional Articular fascial release approach
EXPERIMENTAL3 Dimensional soft tissue release approach
EXPERIMENTALInterventions
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
Hot pack for 15 mins.3- dimensional Articular fascial release approach
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dr Rubina Zulfqar
Faisalabad, Punjab Province, 38000, Pakistan
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
June 9, 2026
First Posted
July 20, 2026
Study Start
July 14, 2026
Primary Completion
August 9, 2026
Study Completion
August 9, 2026
Last Updated
July 23, 2026
Record last verified: 2026-07