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CompletedNCT06519058Updated Dec 17, 2025

Effectiveness of Self-Myofascial Stretching on Carpal Tunnel Syndrome

An interventional study of self-myofascial stretching and conventional physical therapy in Patients With Stage I and II Carpal Tunnel Syndrome, sponsored by Imam Abdulrahman Bin Faisal University. Completed at 1 site in India. Open to participants aged 30 Years to 60 Years. Per ClinicalTrials.gov, last updated 2025-12-17.

Sponsored by Imam Abdulrahman Bin Faisal University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Dec 2023, registered Jun 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
30 Years to 60 Years
Sex
All
01

Study summary

Background/Objectives: Carpal tunnel syndrome (CTS), a median mononeuropathy from nerve compression in the wrist's carpal tunnel, will be studied to compare self-myofascial carpal ligament stretching plus conventional physical therapy versus physical therapy alone for pain reduction and function improvement in stage I/II CTS patients.

Methods: Thirty-six eligible stage I/II CTS patients will be randomized (18/group). The experimental group will receive self-myofascial stretching + conventional therapy; controls will get conventional therapy only. Treatment will last 6 weeks; outcomes will be assessed via Boston Carpal Tunnel Questionnaire and Visual Analogue Scale.

02

Conditions studied

  • Patients With Stage I and II Carpal Tunnel Syndrome
03

In context

Lead sponsor

Imam Abdulrahman Bin Faisal University is the lead sponsor of 88 studies on the registry; 14 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
No

Inclusion criteria

Diagnosed CTS, stage I/II (EMG-confirmed).

Age 30-60 years.

Both genders.

Dominant hand (unilateral/bilateral).

English literate.

Exclusion criteria

Exclusion Criteria:

Polyneuropathy.

Adaptive equipment use.

Shoulder pathologies.

Other neurological/musculoskeletal conditions.

Recent carpal tunnel release (\<1 year).

05

Study design

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

Study arms

  • Experimental
    self-myofascial stretching group

    Other: self-myofascial stretching

  • Sham comparator
    conventional physical therapy group

    Other: conventional physical therapy

Interventions

  • Otherself-myofascial stretching

    self-myofascial stretching exercise

  • Otherconventional physical therapy

    conventional physical therapy treatment, including exercises

06

What researchers measure

Primary outcomes

  1. Boston Carpal Tunnel Questionnaire

    Used to assess the function of carpals

    Time frame: 6 weeks

  2. Visual Analogue Scale

    Involves asking participants to rate their current level of pain on a scale from 0= No pain to 10= maximum pain is felt.

    Time frame: 6 weeks

07

Study locations

1 site
  • Awh special college
    Calicut, India
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06519058
Lead sponsor
Imam Abdulrahman Bin Faisal University
Responsible party
Shibili Nuhmani (Assistant professor, Imam Abdulrahman Bin Faisal University) — Principal investigator
First posted
Jul 25, 2024
Start date
Dec 1, 2023
Primary completion
Feb 4, 2024
Completion
May 29, 2024
Last update
Dec 17, 2025

Study contacts

Shibili Nuhmani, PhD
principal investigator · Imam Abdulrahman Bin Faisal University

Oversight

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 Dec 2025. You cannot join it, but the record below documents what was studied.

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