ClinicalTrials.gg
CompletedNCT06464809Updated Jun 18, 2024

Treatment Intervention of Patients With Carpal Tunnel Syndrome (CTS)

An interventional study of kinesio taping (KT) in Carpal Tunnel Syndrome, sponsored by China Medical University Hospital. Completed at 1 site in Taiwan. Open to participants aged 30 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-18.

Sponsored by China Medical University Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 9 years 8 months after the study started (first participant enrolled Sep 2014, registered Jun 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
30 Years to 60 Years
Sex
All
01

Study summary

The purpose of this study was to investigate the effectiveness of KT versus TENS combining self-myofascial stretching in treatment of CTS through clinical, functional assessment and sensory measurements.

Primary hypothesis The KT group has a more substantial improvement in hand grip, pain relief, enhancing proprioceptive sensitivity and dexterity compare to the TENS group. treatment program,

Read the detailed description

Objective: To compare the effectiveness of a home-based treatment program involving Kinesio taping (KT) or transcutaneous electrical nerve stimulation (TENS) among carpal tunnel syndrome (CTS) patients.

Methods:

30 participants with CTS were enrolled, age range, 30 to 60 years. The participants who met the inclusion criteria were randomized into one of two treatment groups: KT group and TENS group. Participants were blinded to the treatments used in the other group.

Patients with CTS received aforementioned treatments compared with reliable qualitative and quantitative evaluation tools before and after 4-week treatment, as well as at a additional 4-week follow-up. The main parameters include the Symptom Severity Scale (SSS) and Functional Status Scale (FSS), hand grip and key pinch strengths, two-point discrimination (2PD), Modified Moberg pick-up test (MMPUT), and Pain assessment (visual analog scale, VAS).

02

Conditions studied

  • Carpal Tunnel Syndrome

Keywords

  • Carpal tunnel syndrome
  • home-based treatment program
  • kinesio taping
  • paresthesia
  • thenar eminence
03

In context

Carpal Tunnel Syndrome

605 studies on the registry are indexed under Carpal Tunnel Syndrome; 138 are open to participants now.

This study's enrollment of 30 is below the median of 60 across 457 interventional studies indexed under Carpal Tunnel Syndrome.

Browse Carpal Tunnel Syndrome studies →

Lead sponsor

China Medical University Hospital is the lead sponsor of 479 studies on the registry; 115 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • numbness and tingling in the median nerve territory of the hand.
  • nocturnal paresthesia.
  • induction test (Tinel's sign and Phalen's test) showing a positive finding.,
  • is defined as mild and moderate CTS according to nerve conduction studies (NCSs).

Exclusion criteria

Exclusion Criteria:

  • is defined severe CTS symptoms.
  • are currently pregnant or have any secondary entrapment neuropathy (e.g., diabetes, inflammatory arthritis, hypothyroidism, previous wrist trauma).
  • cervical radiculopathy or polyneuropathy.
  • previous history of carpal tunnel decompression surgery.
  • corticosteroid injection into the carpal tunnel.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    kinesio taping (KT) group

    Three precut KT I strips with a width of 5 cm were used. The first strip is applied with the subject's wrist in fully extended hand position. Middle and ring fingers through the holes with the base of the tape as anchored to the knuckles, and then the tape was applied with 15%-25% tension covering the palm and the wrist, and the remainder of the tape without any tension from the wrist up to the forearm. The same process is repeated for the second I-strip, which was applied from the dorsum of the hand to wrist while the wrist in a downward flexed position. The final strip was applied to the carpal tunnel region with 25%-35% tension.

    Other: kinesio taping (KT)

  • Active comparator
    transcutaneous electrical nerve stimulation (TENS) group

    A portable TENS unit (Gem-Stim, Gemore Technology Co., LTD. Taiwan) was used, and delivered a bi-phasic symmetric waveform at a continuous frequency of 100 Hz and phase duration of 200 µsec. The intensity was gradually adjusted up to a strong but comfortable l level, as reported by the subject. Two electrodes were placed 2 cm apart, respectively attached to the carpal ligament of the affected side and the proximal end along the direction of the median nerve.

    Other: kinesio taping (KT)

Interventions

  • Otherkinesio taping (KT)

    Also known as: transcutaneous electrical nerve stimulation (TENS)

06

What researchers measure

Primary outcomes

  1. The SSS and FSS of the Boston Carpal Tunnel Questionnaire (BCTQ)

    Assess symptoms and functional status. The SSS subscale includes 11 items assessing pain, paresthesia, numbness, weakness, nocturnal symptoms and over-all functional status. The FSS subscale includes 8 items assessing the hand function during common daily activities. Each item is scored on a 5-point scale (1-5), from 1(no symptoms) to 5 (the worst symptoms) for SSS, and from 1 (no difficulty) to 5 (cannot perform the activity at all) for FSS. The overall SSS and FSS scores are calculated as the mean of the scores for 11 and 8 individual items respectively, such that the higher the score obtained, the worse the SSS or FSS.

    Time frame: pre-intervention, 4-week intervention, and 4-week follow-up.

  2. Hand grip and key pinch strengths

    pinch strength included palmar, three-jaw chuck, tip, and lateral pinches.

    Time frame: pre-intervention, 4-week intervention, and 4-week follow-up.

  3. Two-point discrimination (2PD)

    cutaneous sensory perception threshold. The larger the value of distance, the worse the sensory ability.

    Time frame: pre-intervention, 4-week intervention, and 4-week follow-up.

  4. Modified Moberg pick-up test (MMPUT)

    hand dexterity. The shorter the time, the more dexterity the hand.

    Time frame: pre-intervention, 4-week intervention, and 4-week follow-up.

  5. The visual analog scale (VAS)

    pain measurement. 100 mm straight line, with 0 mm on the far left and 100 mm on the far right, 0 mm positions It is not painful, and 100 mm is extremely painful.

    Time frame: pre-intervention, 4-week intervention, and 4-week follow-up.

07

Study locations

1 site
  • China Medical University
    Taichung, 406040, Taiwan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06464809
Collaborators
Ministry of Science and Technology, Taiwan
Responsible party
Wei-Hsien Hong (Associate Professor, China Medical University Hospital) — Principal investigator
First posted
Jun 18, 2024
Start date
Sep 24, 2014
Primary completion
Nov 30, 2015
Completion
Dec 30, 2015
Last update
Jun 18, 2024

Study contacts

Wei-Hsien Hong, PhD
principal investigator · China Medical University, Taiwan

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 completed, as verified in Jun 2024. 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