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Effectiveness of Instrument Assisted Soft Tissue Mobilization Technique in De Quervainâ??s Disease

Effectiveness of Instrument Assisted Soft Tissue Mobilization Technique in De Quervainâ??s Diseaseâ??A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/048010
Enrollment
30
Registered
2022-12-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: M654- Radial styloid tenosynovitis [de Quervain]

Interventions

Intervention1: Instrument Assisted Soft Tissue Mobilization (IASTM). : IASTM Treatment plan - 3 sets for 3min/day, and 5 sessions/week for 3 weeks, Total â?? 15 sessions. Control Intervention1: Nume

Sponsors

RANU APEXA RAJESHKUMAR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants with positive Finkelsteinâ??s test, Chronic condition, Participants who are willing to be part of the study.

Exclusion criteria

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 quervainâ??s disease.

Design outcomes

Primary

MeasureTime frame
Numerical pain rating scale (NPRS), Patient-Rated Wrist Evaluation , Goniometer(Smart protractor App). Timepoint: 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.

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactRANU APEXA RAJESHKUMAR

Nootan College of Physiotherapy, Sankalchand Patel University, Visnagar.

dr.srp12345.sp@gmail.com9624692121

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026