Acute Effects of Warm Whirlpool Bath Therapy on Forearm and Hand Muscle Stiffness and Pain in Carpal Tunnel Syndrome

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorErzurum Technical University

About this trial

Carpal tunnel syndrome (CTS) is a common entrapment neuropathy that causes pain, paresthesia and functional limitations in the hand and wrist. Hydrotherapy methods such as warm whirlpool baths are frequently used in physiotherapy practice to reduce pain and improve soft-tissue properties, but their acute effects on forearm and hand muscle stiffness in CTS have not been clearly quantified.

This randomized controlled trial aims to investigate the acute effects of a single session of warm whirlpool bath therapy on forearm and hand muscle stiffness and pain intensity in adults with CTS. Participants diagnosed with CTS will be randomly allocated to an experimental group receiving a 20-minute warm whirlpool bath or to a resting control group. Muscle stiffness of selected forearm and hand muscles will be assessed using the MyotonPRO device, and pain intensity will be recorded with a numeric rating scale, immediately before and after the intervention. It is hypothesized that warm whirlpool bath therapy will produce a greater reduction in muscle stiffness and pain compared with rest alone.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being apparently healthy without a known chronic systemic disease

Physically active participants, regardless of gender

Adults aged 18-65 years diagnosed with carpal tunnel syndrome

No history of other chronic musculoskeletal or neurological disorders

Disqualifiers

Having a previous surgery on the affected wrist or hand

Systemic conditions affecting nerve function, such as diabetes mellitus or thyroid disease

Having a cardiovascular disease or uncontrolled hypertension

Being younger than 18 or older than 65 years

Trial design

Design model

Parallel

Treatments tested in this trial

  • Warm Whirlpool Bath Therapy

    Procedure/Surgery

    The affected hand and forearm are immersed in a therapeutic whirlpool bath with gently circulating water at approximately 38-39°C for 20 minutes. Participants are positioned to ensure comfort and muscle relaxation. Skin integrity and tolerance to heat are checked before treatment and monitored throughout the session

  • Resting Control Condition

    Other intervention

    Participants rest in a comfortable supine or seated position with the affected forearm supported for 20 minutes. No active hydrotherapy, thermal or manual intervention is applied. Positioning and monitoring are comparable to the experimental group.

Treatment groups

24 Participants
are divided into 2 treatment groups
Group A: Warm Whirlpool Bath TherapyExperimental treatment 2 interventions
Group B: Resting ControlActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Primary

Dynamic muscle stiffness (N/m) of selected muscles on the affected upper limb (abductor pollicis brevis, flexor digitorum superficialis, extensor carpi radialis brevis, flexor carpi ulnaris) measured with the MyotonPRO device. For each muscle, three consecutive measurements will be recorded and the mean value will be used for analysis. The primary outcome is the change in stiffness from baseline to post-intervention, compared between the warm whirlpool bath group and the resting control group. Higher values indicate greater muscle stiffness.

Time frame
Baseline (pre-intervention) and immediately after the single 20-minute session (within approximately 5 minutes)

Secondary outcomes

1

Change in Pain Intensity in the Affected Hand/Wrist

Patient-reported pain intensity at the affected hand/wrist assessed using a 0-10 numeric rating scale (0 = no pain, 10 = worst imaginable pain). The primary outcome is the change in pain score from baseline to post-intervention, compared between the warm whirlpool bath group and the resting control group. A decrease in score indicates pain reduction.

Time frame
Baseline (pre-intervention) and immediately after the single 20-minute session (within approximately 5 minutes)

Other outcomes

Sponsors and contacts

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Erzurum Technical University

Lead sponsor

Amasya University

Collaborator

Bangor University

Collaborator

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