The Effects of a Structured Hand Exercise Program on Trigger Finger: A Randomized Controlled Trial
1 other identifier
interventional
76
1 country
1
Brief Summary
To explore the effectiveness of a structured hand exercise program as a conservative treatment for trigger finger.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 28, 2025
CompletedFirst Posted
Study publicly available on registry
April 4, 2025
CompletedStudy Start
First participant enrolled
April 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
ExpectedApril 4, 2025
March 1, 2025
9 months
March 28, 2025
March 28, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Numeric Pain Rating Scale (NPRS) during triggering or movement
NPRS consists of 11-point numeric scale from '0' (no pain) to '10' (worst pain imaginable). Participants rate the pain level based on their own pain intensity from 0-10
Baseline, 6 weeks after baseline, 10 weeks after baseline
Secondary Outcomes (5)
Trigger finger stage in the Green Classification
Baseline, 6 weeks after baseline, 10 weeks after baseline
Frequency of triggering
Baseline, 6 weeks after baseline, 10 weeks after baseline
Functional score by Quick Disabilities of the Arm, Shoulder, and Hand Questionnaire (Hong Kong version)
Baseline, 6 weeks after baseline, 10 weeks after baseline
Grip strength of the affected hand
Baseline, 6 weeks after baseline, 10 weeks after baseline
Structural changes using musculoskeletal ultrasound (A1 pulley thickness, flexor tendon thicknesses, A1 pulley lumen size)
Baseline, 6 weeks after baseline, 10 weeks after baseline
Study Arms (2)
Exercise
EXPERIMENTALControl
NO INTERVENTIONParticipants will receive no intervention.
Interventions
Participants will receive a 6-week structured hand exercise program. Participants will attend a face-to-face exercise session to learn all hand exercises. The exercise program will include: (1) Finger flexor stretching, (2) Tendon gliding exercise and (3) Isometric finger flexor exercise. A weekly tele follow-up will be done to participants in the experimental group
Eligibility Criteria
You may qualify if:
- Adults with aged \> 18 years old who are diagnosed with trigger finger
- The Green classification grade 2 or grade 3
- Pain (NPRS) equal or more than 4/10, during active triggering
You may not qualify if:
- Pediatric or congenital trigger finger
- Previously received physiotherapy, corticosteroid injection or surgery for trigger finger
- Hand trauma, local infection or using systemic steroids due to other diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Hong Kong Polytechnic University
Hong Kong, Hong Kong
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 28, 2025
First Posted
April 4, 2025
Study Start
April 15, 2025
Primary Completion
January 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
April 4, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR
The study data can be provided via contacting the Principal Investigator