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Effects of Low Level Laser Therapy On Exercise Induced Muscle Damage in Wrist Flexors Of Untrained Young Adults

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ClinicalTrials.gov Identifier: NCT04842669
Recruitment Status : Completed
First Posted : April 13, 2021
Last Update Posted : September 30, 2021
Sponsor:
Information provided by (Responsible Party):
Riphah International University

Brief Summary:
The main aim of the current study is to investigate the effects of Low-level Laser Therapy on exercise-induced muscle damage of wrist flexors in untrained young adults. A randomized controlled trial will be conducted at Sargodha Medical College, University of Sargodha. The sample size calculated is 16. The participants will be divided into two equal group; 1) Interventional group (Low level laser therapy), 2) Control group (conventional) each having 8 participants. The study duration will be six months after approval from Research board. Blocked randomization sampling technique will be used. The subjects will be randomly assigned to any of the interventional or control group. Interventional group will further be allocated to prophylactic or therapeutic group. Only Un-trained young Adults, Aged 19-25 (under-graduate/college and university students) without gender discrimination will be included in the study. Tools used in the study will be TALAG Scale (Soreness assessment), Goniometer (ROM), Algometer (Pressure¬-pain Threshold), Electronic digital hand Dynamometer (Grip Strength) and PRS (Perceived Recovery Status Scale). Data will be collected at baseline, 1hr, 24hr, 72hr, 96hr, 120hr, 148hr, 168hr and 192 hrs after the induction protocol.

Condition or disease Intervention/treatment Phase
Wrist Injuries Other: low level laser therapy Other: Conservative treatment Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 20 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Effects of Low Level Laser Therapy On Exercise Induced Muscle Damage in Wrist Flexors Of Untrained Young Adults.
Actual Study Start Date : October 20, 2020
Actual Primary Completion Date : April 20, 2021
Actual Study Completion Date : August 17, 2021

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Low level laser therapy
Low level laser therapy
Other: low level laser therapy
Endo-laser 422 with interchangeable laser probes will be used for the purpose. It is a 2-channel unit and is software operated. For treatment of small surfaces with mono laser there are diodes of 25, 100 and 500 milliWatt.Frequency will be adjusted to 500 Hz, dose 0.1/cm2 with time duration of 1-5 minutes.

Active Comparator: Conservative treatment
Conservative treatment
Other: Conservative treatment
(Topical ibuprofen gel) for muscle soreness will be provided




Primary Outcome Measures :
  1. Numeric pain rating scale (NPRS): [ Time Frame: 8th day (192 hours) ]

    The Numeric Rating Scale is an 11 point scale where the end points are the extremes of no pain and pain as bad as it could be, or worst pain. Numerical Rating Scale has good sensitivity and generates data that can be statistically analyzed for audit purposes.

    Measurements were done at 24, 48, 72, 96,120, 144 and 168, and 192 hours at the same time of the day.


  2. TALAG Scale (Soreness assessment): [ Time Frame: 8th day (192 hours) ]
    TALAG scale will be used to assess the perceived soreness. It consists of points 1-7 on scale. The minimum level 1 with no pain and a maximum point 7 with unbearably painful.Measurement of all dependent variables at 24, 48, 72, 96,120, 144 and 168, and 192 hours after eccentric exercise were taken at the same time of the day.

  3. Goniometer [ Time Frame: 8th day (192 hours) ]
    Physical therapists widely use goniometer for measurement of different joint ranges to evaluate any ROM limitation. The universal full circle goniometer is the preferred instrument for measuring ROM.Measurement of all dependent variables at 24, 48, 72, 96,120, 144 and 168, and 192 hours after eccentric exercise were taken at the same time of the day.

  4. Pressure-pain Threshold by Algometer [ Time Frame: 8th day (192 hours) ]
    Algometer is a reliable tool for measuring pressure pain threshold(22).The Pressure Pain Threshold will be evaluated using an analogue algometer (Baseline, 60 pounds capacity) by applying vertical pressure. To stimulate the participant's pain, the pressure will be increased at a rate of 1kg/cm2.Measurements will be taken pre and post treatment for 2 times during study. Measurement of all dependent variables at 24, 48, 72, 96,120, 144 and 168, and 192 hours after eccentric exercise were taken at the same time of the day.

  5. Electronic digital hand Dynamometer [ Time Frame: 8th day (192 hours) ]
    Grip strength will be evaluated with an electronic digital hand dynamometer as per recommendations. Measurement of all dependent variables at 24, 48, 72, 96,120, 144 and 168, and 192 hours after eccentric exercise were taken at the same time of the day.


Secondary Outcome Measures :
  1. Perceived Recovery (Perceived Recovery Status Scale): [ Time Frame: 8th day (192 hours) ]

    PRS scale is a convenient, noninvasive marker of recovery relative to subsequent training.

    This scale consist of 10 points from 0 -10 with the minimum value 0 for very poorly recovered and maximum 10 value for very well recovered.Measurement of all dependent variables at 24, 48, 72, 96,120, 144 and 168, and 192 hours after eccentric exercise were taken at the same time of the day.




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Ages Eligible for Study:   19 Years to 25 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Un-trained young Adults

Exclusion Criteria:

  • Any Trauma
  • Any psychological condition
  • Participation in any scheduled Physical training
  • Athlete population
  • Use of any nutritional supplement

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04842669


Locations
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Pakistan
Sargodha Medical College (University of Sargodha)
Sargodha, Punjab, Pakistan, 46000
Sponsors and Collaborators
Riphah International University
Investigators
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Principal Investigator: Maria Khalid, MSOMPT Riphah International University
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Responsible Party: Riphah International University
ClinicalTrials.gov Identifier: NCT04842669    
Other Study ID Numbers: REC/00864 Kirran Sikandar
First Posted: April 13, 2021    Key Record Dates
Last Update Posted: September 30, 2021
Last Verified: September 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Riphah International University:
exercise induced muscle damage
wrist flexor
low level laser therapy
Additional relevant MeSH terms:
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Wrist Injuries
Arm Injuries
Wounds and Injuries