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

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

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06911762
Enrollment
76
Registered
2025-04-04
Start date
2025-04-15
Completion date
2026-08-01
Last updated
2025-04-04

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

Conditions

Trigger Finger

Keywords

Trigger finger, tenosynovitis, physiotherapy, conservative treatment, Exercise

Brief summary

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

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

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

* 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

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating Scale (NPRS) during triggering or movementBaseline, 6 weeks after baseline, 10 weeks after baselineNPRS 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

Secondary

MeasureTime frameDescription
Trigger finger stage in the Green ClassificationBaseline, 6 weeks after baseline, 10 weeks after baselineGreen'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)
Frequency of triggeringBaseline, 6 weeks after baseline, 10 weeks after baselineThe 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?
Functional score by Quick Disabilities of the Arm, Shoulder, and Hand Questionnaire (Hong Kong version)Baseline, 6 weeks after baseline, 10 weeks after baselineQuick 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).
Grip strength of the affected handBaseline, 6 weeks after baseline, 10 weeks after baselineGrip 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.
Structural changes using musculoskeletal ultrasound (A1 pulley thickness, flexor tendon thicknesses, A1 pulley lumen size)Baseline, 6 weeks after baseline, 10 weeks after baselineMusculoskeletal ultrasound with a linear transducer (12MHz probe) will be used to evaluate the structural outcome measures.

Countries

Hong Kong

Contacts

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026