Stage-Specific Recovery Changes in the International Classification of Functioning Components Following Conservative Rehabilitation of Trigger Finger

Completed

• Conditions: Trigger Finger
• Interventions: Other: conservative treatment

• Registration Number: NCT05024617
• Lead Sponsor: Hacettepe University

Brief Summary

The aim of this study was to determine the effectiveness of conservative rehabilitation on the multi-dimensional health components based on WHO ICF model in Stage 1, Stage 2 and Stage 3 trigger finger and to determine the functional recovery patterns of each dimension during a three-month rehabilitation period. Thirty-four patients were participated in the study.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2019-03-02
• Primary Completion: 2019-05-20
• Study Completion: 2019-08-31
• Status Verified: 2021-08
• Study First Submitted: 2021-08-24
• Study First Submitted QC: 2021-08-26
• Last Update Submitted: 2021-08-26
• Study First Posted: 2021-08-27
• Last Update Posted: 2021-08-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

• Diagnosed with Stage 1, Stage 2 and Stage 3 trigger finger based on the Froimson Classification

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Exclusion Criteria

• Paediatric trigger finger, trigger thumb, concomitant de'Quervain tenosynovitis, carpal tunnel syndrome, or Dupuytren's contracture, neurological or rheumatological diseases, chronic pain syndromes, pregnancy and patients with treatment history of related finger/fingers.

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
trigger finger stage 1-2-3	conservative treatment	Volunteer patients between 35-65 years old diagnosed with Stage 1, Stage 2 and Stage 3 trigger finger based on the Froimson Classification were included in the study. Exclusion criteria include paediatric trigger finger, trigger thumb, concomitant de'Quervain tenosynovitis, carpal tunnel syndrome, or Dupuytren's contracture, neurological or rheumatological diseases, chronic pain syndromes, pregnancy and patients with treatment history of related finger/fingers

Primary Outcome Measures

Name	Time	Method
Pain (VAS)	one month
Number of triggering (ten active fist test / 30 second active fist test)	one month
Grip strength (hand dynomometer and pinchmeter)	one month

Trial Locations

Locations (1)

Hacettepe University Faculty of Physical Therapy and Rehabilitation; 🇹🇷 Ankara, Turkey