Actively Recruiting

Phase Not Applicable
Age: 21Years - 50Years
All Genders
NCT06839690

Comparison of Sub-maximal Voluntary Isometric Training vs Eccentric Training in Management of De Quervain Tenosynovitis

Led by Foundation University Islamabad · Updated on 2025-02-21

58

Participants Needed

1

Research Sites

48 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a randomised control trial and the purpose of this study is to compare the effects of Sub-maximal Voluntary Isometric Training vs Eccentric Training in Management of De Quervain Tenosynovitis

CONDITIONS

Official Title

Comparison of Sub-maximal Voluntary Isometric Training vs Eccentric Training in Management of De Quervain Tenosynovitis

Who Can Participate

Age: 21Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with thumb pain or tenderness lasting 3 weeks or more
  • Age between 21 and 50 years
  • All genders eligible
  • Score 3 or more out of 7 on De Quervain screening tool
  • Positive Wrist hyperflexion and abduction of thumb (WHAT) test
  • Positive Finkelstein's / Eichhoff's test
Not Eligible

You will not qualify if you...

  • Diagnosed osteoarthritis of the 1st CMC joint or rheumatoid arthritis
  • C6 cervical radiculopathy
  • Any systemic inflammatory condition such as septic arthritis
  • Carpal Tunnel Syndrome
  • Complex regional pain syndrome
  • Previous surgery affecting the first extensor compartment of the wrist
  • Corticosteroid injection in the radial wrist area within 3 months before study entry
  • Previous isometric thumb exercises or strengthening protocols longer than 2 weeks for current De Quervain's episode

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Foundation University College of Physcial Therapy

Rawalpindi, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

Z

Zahra Nayyer, MS-MSKPT*

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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