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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05100394
Other study ID # RRC-2021-07
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 5, 2021
Est. completion date September 23, 2021

Study information

Verified date October 2021
Source King Saud University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Proximal hamstring tendinopathy (PHT) is tendinopathy of the semimembranosus and/or biceps femoris/semitendinosus complex. Previous studies have shown the efficacy of laser therapy in the treatment of tendinopathy. To the best of the investigator's knowledge, no study has compared the effects of high-power LASER therapy with conventional physiotherapy programs in proximal hamstring tendinopathy patients. Therefore, this study aimed to assess the effects of high-power laser therapy on pain and muscle power in proximal hamstring tendinopathy patients.


Description:

2 arms comparative pretest-posttest experimental research design with random allocation of subjects into groups (experimental and control group) using the lottery method. A total of thirty-six participants aged between 18-35 (mean age) years, were recruited in the present study. The selected participants were randomly allocated into experimental and control groups using the lottery method and website randomization.com with eighteen participants in each group. The participants and outcome assessor were kept blinded to the allocation. In the experimental group, the high-power laser was given whereas in the control group conventional physiotherapy treatment was given for 4 weeks. Conventional physiotherapy treatment included the US, moist heat pack, and home exercises. Home exercises include nordic hamstring exercises - 2 sets of 5 repetitions, 3 days/week for 3 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date September 23, 2021
Est. primary completion date August 27, 2021
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Athletes - pain located deep in the buttock/posterior thigh region - tenderness of ischial tuberosity - hamstring muscle tightness. Exclusion Criteria: - Recent trauma to the posterior thigh - Musculoskeletal disorder of ipsilateral lower extremity - taking pain medication daily - hypertension, malignancy, autoimmune disease, phlebitis, blood disorder.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Laser Therapy
Therapeutic laser therapy was applied.
Other:
Ultrasound + Moist Heat pack + Exercises
Ultrasound therapy, a moist heat pack, and a home exercise program were given.

Locations

Country Name City State
Saudi Arabia King Saud University Riyadh

Sponsors (1)

Lead Sponsor Collaborator
King Saud University

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numerical Pain Rating Scale On a scale of 0-10, patients rate their current pain level. Higher scores mean worse outcome. 3 weeks.
Primary Isokinetic peak torque Isokinetic muscle power was measured. 3 weeks.
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