Skip to content

The effectiveness of manual therapy of shoulder trigger points on pain and disability in patients with carpal tunnel syndrome

Evaluation of the effectiveness of periscapular trigger points deactivation on pain and disability in patients with carpal tunnel syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014071915932N6
Enrollment
30
Registered
2014-08-14
Start date
2014-08-29
Completion date
Unknown
Last updated
2018-02-22

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: Patients in control group received 10 sessions of physical therapy at the wrist area as the following: -Therapeutic ultrasound for 3 min with a continuous 3.0 MHz applicator, ERA = 5
Rehabilitation
Patients in control group received 10 sessions of physical therapy at the wrist area as the following: -Therapeutic ultrasound for 3 min with a continuous 3.0 MHz applicator, ERA = 5 cm2, intensity
Patients in intervention group received 10 sessions of physical therapy at the wrist area as the following: -Therapeutic ultrasound for 3 min with a continuous 3.0 MHz applicator, ERA = 5 cm2, inte

Sponsors

Shiraz University of Medical Sciense
Lead Sponsor

Eligibility

Sex/Gender
All
Age
24 Years to 60 Years

Inclusion criteria

Inclusion criteria: inclusion criteria:patients with CTS syndrome for more than 1 month; positive Tinne'sl sign at the wrist area; positive Phalen's test; mild to moderate carpal tunnel syndrome by electrodiagnostic findings; existence of trigger points in at least two periscapular muscles( teres minor& major? supraspinatus? infraspinatus? subscapularis? upper trapezius ); aged between 24 to 60 years. exclusion criteria:any neuropathy such as diabetic neuropathy; thoracic outlet syndrome; cervical disk herniation; double crush syndrome( positive neck compression test); regular use of analgesics or anti-inflammatory drugs; Pregnancy; Rheumatoid Arthritis; history of physical therapy, surgery or steroid injection for the treatment of CTS; history of treatment for periscapular trigger points such as steroid injection in last 3 months; fibromyalgia; T4 syndrome.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Power grip. Timepoint: First and tenth session. Method of measurement: Be assessed by hand-held dynamometer.;Pain. Timepoint: First and tenth session. Method of measurement: Visual analogue scale.;Sensitivity of periscapular trigger points. Timepoint: First and tenth session. Method of measurement: algometry.;Functional disability. Timepoint: First and tenth session. Method of measurement: DASH questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactForouzan Foroughi

Shiraz University of Medical Science - Rehablitation School.

foroughi.forouzan13@gmail.com+98 71 1843 1416

Outcome results

None listed

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