Laser Therapy on Hamstring Muscle Among Young Adults

October 9, 2023 updated by: Asir John Samuel, Maharishi Markendeswar University (Deemed to be University)

High-intensity Laser Therapy on Hamstring Muscle Length Among Young Adults

A total of 154 healthy young individuals will be recruited by purposive sampling method to participate in a randomized, single-blinded, sham-controlled study. Recruited participants will be randomly dividing into two groups, the Active high-intensity laser therapy (a-HILT) group, and the Sham high-intensity laser therapy (s-HILT) group. The treatment duration will be 10 minutes per session on both lower limbs for each day for 3 days/week for 2 weeks. Hamstring muscle length will be assessed at baseline, end of the 2-week post-intervention period.

Study Overview

Study Type

Interventional

Enrollment (Actual)

136

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Haryana
      • Ambāla, Haryana, India, 133207
        • Maharishi Markandeshwar (M.M) Hospital, Mullana, Ambala, Haryana

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Asymptomatic young adults
  • Both gender
  • Tightness of hamstring muscles

Exclusion Criteria:

  • Any other musculoskeletal disorder
  • Any disc pathology
  • Any nerve root irritation
  • Any surgical history or trauma
  • Malignancy
  • Pregnancy
  • Sensory dysfunctions
  • Cardiac pacemaker

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: High-intensity laser therapy
77 participants will receive active high-intensity laser therapy interventions on hamstring muscle to improve the flexibility of muscle

High-intensity laser therapy will be used in the contact method, with the laser beam irradiated over the hamstring muscle. Dosage and parameters for the laser will be calculated.

Parameters-

  1. Wavelength- 980 nm
  2. Intensity/Power density- 3W/cm2
  3. Emission mode- Continuous Emission
  4. Energy (Joules)- 490 J
  5. Irradiation time- 70 Sec on each point
  6. Peak power- 15 Watt
  7. Irradiation points- 09
Sham Comparator: Sham High-intensity laser therapy
77 participants will receive sham high-intensity laser therapy on hamstring muscle
Sham High-intensity laser therapy will be used in the contact method, without the laser beam irradiation over the hamstring muscle.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Active Knee Extension Test
Time Frame: Changes will be measured at baseline, end of two week post intervention
Active knee extension test (AKET) is most reliable method to assess the hamstring tightness.
Changes will be measured at baseline, end of two week post intervention
Sit and toe touch test
Time Frame: Changes will be measured at baseline, end of two week post intervention
Sit and toe touch test is used to assess the hamstring flexibility
Changes will be measured at baseline, end of two week post intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Adarsh K Srivastav, PhD Scholar, MMIPR, MM(DU)
  • Study Director: Asir J Samuel, PhD, MMIPR, MM(DU)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2022

Primary Completion (Actual)

August 19, 2023

Study Completion (Actual)

October 9, 2023

Study Registration Dates

First Submitted

October 1, 2021

First Submitted That Met QC Criteria

October 1, 2021

First Posted (Actual)

October 14, 2021

Study Record Updates

Last Update Posted (Estimated)

October 10, 2023

Last Update Submitted That Met QC Criteria

October 9, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • U1111-1269-9595

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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