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Investigating the effect of concurrent myofascial release of the shoulder girdle and hand compared to myofascial release of the hand on functional and electrodiagnostic parameters of patients with mild and moderate carpal tunnel syndrome

Investigating the effect of concurrent myofascial release of the shoulder girdle and hand compared to myofascial release of the hand on functional and electrodiagnostic parameters of patients with mild and moderate carpal tunnel syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250222064806N1
Enrollment
45
Registered
2025-05-07
Start date
2025-05-05
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Carpal Tunnel Syndrome. Carpal tunnel syndrome

Interventions

Intervention 1: Intervention group 1: concurrent myofascial release of the shoulder girdle and hand

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Age: 18-50 years old Mild & moderate idiopathic CTS VAS above 3

Exclusion criteria

Exclusion criteria: Cervical radiculopathypoly Polyneuropathy Diabetes mellitus Hypothyroidism Chronic kidney failure Chronic alcoholism Acromegaly Connective tissue disease Inflammatory diseases Pregnant Breast feeding History of fracture or surgery in the hand More than 20% absence in practice sessions Unwillingness to continue

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: After the initial evaluation, individuals in all three groups will undergo 10 treatment sessions, 3 sessions per week for 4 weeks. Four weeks after the last treatment session, the evaluations will be repeated and the results will be reviewed. Method of measurement: Visual Analog Scale(VAS).;Function. Timepoint: After the initial evaluation, individuals in all three groups will undergo 10 treatment sessions, 3 sessions per week for 4 weeks. Four weeks after the last treatment session, the evaluations will be repeated and the results will be reviewed. Method of measurement: Boston CTS questionnaire.;Myofascial Release. Timepoint: After the initial evaluation, individuals in all three groups will undergo 10 treatment sessions, 3 sessions per week for 4 weeks. Four weeks after the last treatment session, the evaluations will be repeated and the results will be reviewed. Method of measurement: Manual.;Nerve Conduction Velocity. Timepoint: After the initial evaluation, individuals in all three groups will undergo 10 treatment sessions, 3 sessions per week for 4 weeks. Four weeks after the last treatment session, the evaluations will be repeated and the results will be reviewed. Method of measurement: Electrodiagnostic studies with an EMG device.;Latency. Timepoint: After the initial evaluation, individuals in all three groups will undergo 10 treatment sessions, 3 sessions per week for 4 weeks. Four weeks after the last treatment session, the evaluations will be repeated and the results will be reviewed. Method of measurement: Electrodiagnostic studies with an EMG device.;Amplitude. Timepoint: After the initial evaluation, individuals in all three groups will undergo 10 treatment sessions, 3 sessions per week for 4 weeks. Four weeks after the last treatment session, the evaluations will be repeated and the results will be reviewed. Method of measurement: Electrodiagnostic studies with an EMG device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Mokhtari

Semnan University of Medical Sciences

azadehmokhtari27@gmail.com+98 23 3365 4180

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026