CClinicalTrials.gg
Not yet recruitingNCT06911762Updated Apr 4, 2025

The Effects of a Structured Hand Exercise Program on Trigger Finger: A Randomized Controlled Trial

An interventional study of Exercise in Trigger Finger, sponsored by The Hong Kong Polytechnic University. Not yet recruiting at 1 site in Hong Kong. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-04-04.

Sponsored by The Hong Kong Polytechnic University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
76
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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

02

Conditions studied

  • Trigger Finger

Keywords

  • Trigger finger
  • tenosynovitis
  • physiotherapy
  • conservative treatment
  • Exercise
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • 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
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
76 participants (estimated)

Study arms

  • Experimental
    Exercise

    Behavioral: Exercise

  • No intervention
    Control

    Participants will receive no intervention.

Interventions

  • BehavioralExercise

    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

05

What researchers measure

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

    Time frame: Baseline, 6 weeks after baseline, 10 weeks after baseline

Secondary outcomes

  1. Trigger finger stage in the Green Classification

    Green's classification for trigger finger: Grade 1 (A history of catching with local pain). Grade 2 (Demonstrable catching with normal active extension). Grade 3 (Demonstrable locking requiring passive extension). Grade 4 (Fixed flexion deformity)

    Time frame: Baseline, 6 weeks after baseline, 10 weeks after baseline

  2. Frequency of triggering

    The frequency of triggering will be represented by the number of triggering events in ten active fists, from 0 to 10. Two questions will be asked: (1) What is the average number of triggering in ten active fists in the past one week? (2) What is the average number of painful triggering in ten active fists in the past one week?

    Time frame: Baseline, 6 weeks after baseline, 10 weeks after baseline

  3. Functional score by Quick Disabilities of the Arm, Shoulder, and Hand Questionnaire (Hong Kong version)

    Quick Disabilities of the Arm, Shoulder, and Hand Questionnaire (QuickDASH) is a shorten version of the Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH). QuickDASH consisted of 11 items to measure physical function and symptoms in patients with upper limb disorders. DASH and QuickDASH were translated into Hong Kong version. Participants must complete at least 10 of the 11 items for a score to be calculated and the scores range from 0 (no disability) to 100 (most severe disability).

    Time frame: Baseline, 6 weeks after baseline, 10 weeks after baseline

  4. Grip strength of the affected hand

    Grip strength will be assessed using the American Society of Hand Therapists (ASHT) protocol. Participants will be seated in a chair without arm rests, with hips and knees in 90 degrees. Shoulder holds in adduction and neutral rotation. Elbow holds in 90 degrees flexion with forearm in neutral rotation. Participants grip the dynamometer in 15-30 degrees wrist extension and 0-15 degrees of ulnar deviation. Participants will be asked to grip the dynamometer as hard as they can for 3 trials. The mean of the 3 trials will be recorded as the grip strength in kg.

    Time frame: Baseline, 6 weeks after baseline, 10 weeks after baseline

  5. Structural changes using musculoskeletal ultrasound (A1 pulley thickness, flexor tendon thicknesses, A1 pulley lumen size)

    Musculoskeletal ultrasound with a linear transducer (12MHz probe) will be used to evaluate the structural outcome measures.

    Time frame: Baseline, 6 weeks after baseline, 10 weeks after baseline

06

Study locations

1 site
07

References and documents

Individual participant data

Plan to share: Yes — The study data can be provided via contacting the Principal Investigator

Supporting information: Study protocol, Sap, Icf, Csr

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06911762
Lead sponsor
The Hong Kong Polytechnic University
Responsible party
Freddy Man Hin LAM (Assistant Professor, The Hong Kong Polytechnic University) — Principal investigator
First posted
Apr 4, 2025
Start date
Apr 15, 2025 (estimated)
Primary completion
Jan 1, 2026 (estimated)
Completion
Aug 1, 2026 (estimated)
Last update
Apr 4, 2025

Study contacts

Freddy Man Hin LAM, PhD
Contact
freddy-mh.lam@polyu.edu.hk
+852 2766-6720

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion