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The Effects of TECAR Therapy in Athletes with Longstanding Adductor Related Groin Pain

The Effects of TECAR Therapy on Pain, Range of Motion, Strength and Subscale of The Copenhagen Hip and Groin Outcome Scale Questionnaire in Athletes with Longstanding Adductor Related Groin Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220622055250N1
Enrollment
22
Registered
2022-09-18
Start date
2022-09-23
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Adductor Related Groin Pain.

Interventions

Intervention group: The people who are in this group will receive ten sessions treatment in three times a week. In this group, the TECAR device will be used with the aim of heating the tissues for 15

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Athletes with Adductor related groin pain, at least one month after the injury Unilateral Injury of Adductor Muscles Ability to Read and Write in Persian language (Elementary First Period) Age 18-45 Tenderness in Adductor Muscles Pain during Resistance Test of Adductor Muscles Pain at the Beginning of the Study Should be 3-7. (Based on Visual Analogue Scale) Injury confirmation by a Sports Specialist Doctor

Exclusion criteria

Exclusion criteria: Unwillingness to Continue Treatment Suffering from Injuries and Fractures in the Lower Limbs in a Way that Prevents the Completion of the Treatment Process Urinary and Genital Infections Hernia (inguinal, femoral) Referral Pains to the Groin Area Malignant tumors Accompanying Problems in the Groin Area Received Treatment in the Last 1 Month Cases of Non-use of the TECAR Therapy Device Include Pregnancy, Tumor, Electrical Devices Placed Inside the Body Such as Cardiac Pacemaker, Fever, Having Transplanted Tissue.

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: First session, session 6, session 10, After 1 month. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Physical function, daily living. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: The Copenhagen Hip and Groin Outcome Score Questionnaire.;Range of Motion. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: Goniometer.;Strength. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: Dynamometer.;Quality of Life. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: The Copenhagen Hip and Groin Outcome Score Questionnaire.;Pain. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: The Copenhagen Hip and Groin Outcome Score Questionnaire.;Symptoms. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: The Copenhagen Hip and Groin Outcome Score Questionnaire.;Participation in physical activities. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: The Copenhagen Hip and Groin Outcome Score Questionnaire.;Function, sports and recreational activities. Timepoint: First session, Session 6, Session 10, After 1 month. Method of measurement: The Copenhagen Hip and Groin Outcome Score Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Nazari

Iran University of Medical Sciences

nazari.sara@iums.ac.ir+98 21 2222 7124

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026