Skip to content

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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07714031
Enrollment
46
Registered
2026-07-20
Start date
2026-07-14
Completion date
2026-08-09
Last updated
2026-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wrist Joint Overuse Syndrome

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.

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

Sponsors

University of Faisalabad
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
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

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

Design outcomes

Primary

MeasureTime frameDescription
Pain Intensity3 weeksPain 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.
Range of Motion3 weeksRange of Motion will be measured by using Goniometry the improvement in ROM shows good results.

Secondary

MeasureTime frameDescription
Functional disability3 weeksFunctional 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.

Countries

Pakistan

Contacts

CONTACTDr Rubina Zulfqar
drrubinazulfqar355@gmail.com+923414291664

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 24, 2026