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Developing screening method for de quervains tenosynovitis among computer users.

Developing screening tool for de Quervain tenosynovitis among computer users. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/03/063488
Enrollment
300
Registered
2024-03-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

None listed

Interventions

Intervention1: Computer User Screening for De Quervains Tenosynovitis: A Prospective Study: Screening tool development, participant recruitment, informed consent and baseline assessment, screening imp

Sponsors

Jeet Dey
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Computer usage more than 5 hours for 5 to 6 days in a week, diagnosed case of de quervain since 1 month, presence of pain and discomfort in thumb region, pain worsen during work and difficulty in gripping objects, numeric pain rating scale less than 7 and patients willing to participate

Exclusion criteria

Exclusion criteria: Previous history of wrist trauma or surgery, Rheumatoid arthritic patients, patients having any neurological deficits, patients on any pain reliving medication since 1 month, person having any congenital deformity, patients outside the age bracket, and patients not willing to participate.

Design outcomes

Primary

MeasureTime frame
To create a rapid assessment tool that aids in prompt identification and treatment of the disease. Timepoint: 6 months

Secondary

MeasureTime frame
Cost effectivenessTimepoint: 8 weeks

Countries

India

Contacts

Public ContactRabab Kaur

Amity University Noida

rkaur4@amity.edu9654478155

Outcome results

None listed

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