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Comparison of Intermittent Occlusion and Static Stretching

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04574661
Recruitment Status : Completed
First Posted : October 5, 2020
Last Update Posted : February 17, 2021
Sponsor:
Information provided by (Responsible Party):
Riphah International University

Brief Summary:
To determine changes in Vitals caused by Intermittent Occlusion ( 220 mg ) and to compare the effectiveness of Intermittent Occlusion and Static Stretching of the lower limb muscle group in preventing the development of exercise induce Muscle Soreness

Condition or disease Intervention/treatment Phase
Muscle Soreness Other: Static Stretching Other: Intermittent Occlusion Not Applicable

Detailed Description:

Main purpose of this study is to determine changes in Vitals caused by Intermittent Occlusion ( 220 mg ) and to compare the effectiveness of Intermittent Occlusion and Static Stretching of the lower limb muscle group in preventing the development of exercise induce Muscle Soreness. As muscle soreness is very major and basis problem of every individual , specially after enrolling into some physical activity .

First consent form will be given to both male and female participants from 18 to 25 years of age and after that PAR-Q Questionnaire will be filled for every individual, so that we will check their readiness for the Exercise then all the four Vitals will measured from every individual .They will randomly assigned by lottery method to intervention group and control group. Both group individuals will be exerted by Warm up for 5 mints, heel raise in 3 sets for 10 to 15 mints until we get 4 on RPE scale, by asking to hold dumbbells of 2 kg on both of the hands. Rate of perceived exertion (RPE) is calculated by Borg grading scale .Plus, leg circumference, ROM of planter and dorsal flexion and numeric pain rating scale (NPRS) will be measured for comparison within and between the groups. Again vitals will be monitored.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 20 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Prevention
Official Title: Comparison of Intermittent Occlusion and Static Stretching of Muscles in Prevention of Soreness and Vital Changes in Young Adults
Actual Study Start Date : January 15, 2020
Actual Primary Completion Date : September 30, 2020
Actual Study Completion Date : September 30, 2020

Arm Intervention/treatment
Active Comparator: Static stretching
Static stretching to lower limb muscles
Other: Static Stretching
In Control group all the individuals will be asked to perform static stretching for 10 mints, 1 set . Vitals will be monitored from every individual. On 3rd day to this protocol leg circumference, ROM of planter and dorsal flexion and numeric pain rating scale (NPRS ) will be measured alone with all the Vitals from every individual.

Experimental: Intermittent occlusion
Intermittent occlusion to lower limb
Other: Intermittent Occlusion
Individuals of Interventional group will be asked to lay down in supine position, apply proximal thigh cuff, 220mg for 12 minutes for intermittent occlusion. During this procedure discomfort will be checked on numeric pain rating scale, if we get 6 on scale, will stop the occlusion. Vitals will be monitored from every individual. On 3rd day to this protocol leg circumference, ROM of planter and dorsal flexion and numeric pain rating scale (NPRS ) will be measured alone with all the Vitals from every individual




Primary Outcome Measures :
  1. Numeric pain rating scale (NPRS) [ Time Frame: 4th day ]
    The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain). It has been shown that a composite scoring system including best, worse, and current level of pain. 27 Recent studies showed that the Majority of patients of all ages and both genders prefer NRS 28. Patients feel this scale of pain measuring technique quite easy and understandable. The benefit of the NRS is that it is validated as well as quick and easy to use.

  2. Goniometer [ Time Frame: 4th day ]
    A goniometer is an instrument which measures the available range of motion at a joint. This can be an indicator of stress which is unavoidable. Many studies showed that The universal goniometer are reliable in repeated measures of joint angles 30 .Manual goniometers can be used with confidence for longitudinal assessments in the clinic

  3. Measuring Tape [ Time Frame: 4th day ]
    Tape measurement has been used for decades round measurement or the contour of the Muscle to detect atrophy or hypertrophy of Joint to determine swelling. Research shows that measuring tape is valid and reliable tool for circumference measurements .Circumference measurements taken by spring tape have high reliability

  4. Borg Rate of Perceived Exertion [ Time Frame: 4th day ]
    Research suggest that the Borg CR-10 scale is valid and reliable for monitoring exercise intensity

  5. PAR-Q Questionnaire [ Time Frame: 4th day ]
    Physical Activity Readiness Questionnaire (PARQ) clearance has been recommended prior to low-to-moderate exercise involvement. Physical Activity Readiness Questionnaire (PARQ) is safe and effective means of risk stratification for patients interested in becoming more physically active. These results support the concurrent validity of the PARQ and suggest the revisions have had their intended effect

  6. Temperature [ Time Frame: 4th day ]
    A valid Tool for temperature measurement which has been in use from centuries is Mercury Thermometer.

  7. Pulse rate [ Time Frame: 4th day ]
    The pulse rate is a measurement of the heart rate, or the number of times the heart beats per minute which can be felt by the beats by firmly pressing on the arteries, which are located close to the surface of the skin at certain points of the body. In this study we will be using Radial Artery.

  8. Respiratory Rate [ Time Frame: 4th day ]
    The respiration rate is the number of breaths a person takes per minute , when a person is at rest counting the number of breaths for one minute by counting how many times the chest rises.

  9. Blood pressure [ Time Frame: 4th day ]
    The aneroid monitor is valid and cost effective tool which for measuring blood pressure



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Ages Eligible for Study:   18 Years to 25 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Age limit: 18 -25 years of age.
  • Both Males and Females.
  • Participants intending to join a fitness or body building program shortly ( the first exercise session would be utilized to induce mild muscle soreness )
  • Participants ready for physical exertion according to PAR-Q.

Exclusion Criteria:

  • Obesity (body mass index ≥ 30 kg/m2).
  • Skeletal or Orthopedic Injuries.
  • Known Cardiovascular disease.
  • Open wounds.
  • Uncontrolled Hypertension (resting brachial blood pressure ≥ 140/90 mmHg).
  • Exercise induced muscle soreness in last 6 months.

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): NCT04574661


Locations
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Pakistan
Shalimar Club
Rawalpindi, Punjab, Pakistan, 46000
Sponsors and Collaborators
Riphah International University
Investigators
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Principal Investigator: Anam Aftab, Phd* Riphah college of rehabilitation and allied health sciences - Rawalpindi
Publications:

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Responsible Party: Riphah International University
ClinicalTrials.gov Identifier: NCT04574661    
Other Study ID Numbers: REC/00240 Urooj Fatima
First Posted: October 5, 2020    Key Record Dates
Last Update Posted: February 17, 2021
Last Verified: February 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:
Muscle soreness
Vital Signs
Intermittent occlusion
Static stretching
Additional relevant MeSH terms:
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Myalgia
Muscular Diseases
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases
Musculoskeletal Pain
Pain
Neurologic Manifestations