Effectiveness of Instrument Assisted Soft Tissue Mobilization Technique in De Quervain’s Disease

Not yet recruiting

• Conditions: Radial styloid tenosynovitis [de Quervain],

• Registration Number: CTRI/2022/12/048010
• Lead Sponsor: RANU APEXA RAJESHKUMAR

Brief Summary

TITLE- Effectiveness of Instrument Assisted Soft Tissue Mobilization Technique in De Quervain’s Disease–A Randomized Controlled Trial

INVESTIGATOR NAME - RANU APEXA RAJESHKUMAR (BPT INTERN) ,Nootan College of Physiotherapy, Sankalchand Patel University, Visnagar, 384315.

AIM - The aim of this study is to find out the effectiveness of the Instrument assisted soft tissue mobilization in De Quervain’s Disease.

OBJECTIVES -

To decrease pain,

To improve range of motion,

To restoring proper function,

To compare the experimental group to the control group.

MATERIALS -

Assessment Form

Consent Form

Goniometer (Smart protractor app)

Functional outcome index

Instrument assisted soft tissue mobilization tool

Pen & paper

Pillow

Laptop

Chair

PROCEDURE

The research will be done after approved by the ethics committee of Nootan Collage of Physiotherapy, Sankalchand Patel University, Visnagar. First, all participants will be educated about the study processes and the participants will be asked to give their written consent and permit participation in this study.

The study population will consist of 30 participants who had De Quervain’s Tenosynovitis.

The participants will randomly be allocated into two groups: an experimental group (n-15) and a control group (n-15).

The physical characteristics of the all participants will recorded at the outset of the study.

The participants who will allocated to the experimental group will receive IASTM treatment

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2022-09-12
• Study Start: 2022-12-12

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Participants with positive Finkelstein’s test, Chronic condition, Participants who are willing to be part of the study.

Exclusion Criteria

Participants with carpal tunnel syndrome, Participants with any arthritic changes like Rheumatoid arthritis, Participants with any fracture and deformity in wrist, Participants with radiating pain and other neurological signs, Pregnancy, Prior surgery for de quervain’s disease.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Numerical pain rating scale (NPRS),	Numerical pain rating scale (NPRS), | Patient-Rated Wrist Evaluation, | Goniometer (Smart protractor App). | These all outcome measures will be assessed before the treatment began and after completion of the 3 weeks of IASTM treatment session again all outcomes will be re-assessed.
Patient-Rated Wrist Evaluation ,	Numerical pain rating scale (NPRS), | Patient-Rated Wrist Evaluation, | Goniometer (Smart protractor App). | These all outcome measures will be assessed before the treatment began and after completion of the 3 weeks of IASTM treatment session again all outcomes will be re-assessed.
Goniometer(Smart protractor App).	Numerical pain rating scale (NPRS), | Patient-Rated Wrist Evaluation, | Goniometer (Smart protractor App). | These all outcome measures will be assessed before the treatment began and after completion of the 3 weeks of IASTM treatment session again all outcomes will be re-assessed.

Trial Locations

Locations (1)

Nootan College of Physiotherapy.; 🇮🇳 Mahesana, GUJARAT, India

Nootan College of Physiotherapy.

🇮🇳Mahesana, GUJARAT, India

RANU APEXA RAJESHKUMAR

Principal investigator

6354654769

arranu434@gmail.com