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Effect of Fatih massage on carpal tunnel syndrome

Study of the effect of Fatih traditional manual therapy on patients with mild and moderate carpal tunnel syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190429043421N1
Enrollment
34
Registered
2019-07-22
Start date
2019-05-22
Completion date
Unknown
Last updated
2019-10-07

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: Part I: Hack (a specific movement in Iranian massage) on the shoulder, circular and fast moving for 2 minutes, then Hack on the posterior neck with circular motion

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 20-60 years old; clinical diagnosis by a physical medicine specialist and confirmed by electrical diagnosis (EMG&NCV); mild to moderate disease; at least 3 months after the onset of the symptoms; informed consent and accepting the terms of participation in the research.

Exclusion criteria

Exclusion criteria: A history of trauma or surgery Recent treatment history, including physiotherapy, laser therapy, or any injection such as steroid in the carpal tunnel region within the past 2 months Pregnancy The history of diabetes and thyroid dysfunction according to the patient's own announcement Median nerve involvement in areas other than the Carpal tunnel area, which is diagnosed with clinical diagnosis of physical medicine and NCV History of vascular collagen diseases such as rheumatoid arthritis, scleroderma, amyloidosis, lupus Coincidence with other known tenosynovitis that has been approved by the rheumatologist Presence of Advanced Cancer or Recent Chemotherapy and Radiation Therapy Use of anticancer drugs, corticosteroids, immunosuppressive drugs and cytotoxic drugs Severe medical conditions, such as renal and cardiac failure, obesity or overweight (based on BMI) Items outside the range of mild to moderate (mentioned in the criteria for entry) with symptoms such as Tenar muscle atrophy and the presence of permanent paresthesia

Design outcomes

Primary

MeasureTime frame
Boston Questionnaire Score (Boston Symptoms and Functional Capacity Scale). Timepoint: The beginning of the study and the 2nd, 4th, 8th and 10th weeks. Method of measurement: Boston Questionnaire.;Electrophysiological tests (neural conduction study). Timepoint: The beginning of the study and the tenth week. Method of measurement: nerve conduction velocity (NCV) test & Electromyography (EMG).;Evaluation of pain. Timepoint: The beginning of the study and the tenth week. Method of measurement: Pain scale.

Secondary

MeasureTime frame
Satisfaction Satisfaction Assessment. Timepoint: Tenth week. Method of measurement: Satisfaction Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoshanak Mokaberinejad

Shahid Beheshti University of Medical Sciences

mokaberi@sbmu.ac.ir+98 21 8877 3521

Outcome results

None listed

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