NCT06911762

Brief Summary

To explore the effectiveness of a structured hand exercise program as a conservative treatment for trigger finger.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
76

participants targeted

Target at P50-P75 for not_applicable

Timeline
3mo left

Started Apr 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress82%
Apr 2025Aug 2026

First Submitted

Initial submission to the registry

March 28, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 4, 2025

Completed
11 days until next milestone

Study Start

First participant enrolled

April 15, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2026

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Expected
Last Updated

April 4, 2025

Status Verified

March 1, 2025

Enrollment Period

9 months

First QC Date

March 28, 2025

Last Update Submit

March 28, 2025

Conditions

Keywords

Trigger fingertenosynovitisphysiotherapyconservative treatmentExercise

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

EXPERIMENTAL
Behavioral: Exercise

Control

NO INTERVENTION

Participants will receive no intervention.

Interventions

ExerciseBEHAVIORAL

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

Exercise

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Trigger Finger DisorderTenosynovitisMotor Activity

Interventions

Exercise

Condition Hierarchy (Ancestors)

Tendon EntrapmentTendinopathyMuscular DiseasesMusculoskeletal DiseasesBehavior

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Central Study Contacts

Freddy Man Hin LAM, PhD

CONTACT

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

The study data can be provided via contacting the Principal Investigator

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR

Locations