Dynamic Oscillatory Stretch Technique Versus Static Stretching In Reduced Hamstring Flexibility

August 7, 2019 updated by: Riphah International University

Comparison Between Dynamic Oscillatory Stretch Technique and Static Stretching In Reduced Hamstring Flexibility in Healthy Population: A Single Blind Randomized Control Trial

This study compared the effects of dynamic oscillatory stretch technique (DOS) and static stretching (SS) technique in order to improve hamstring extensibility in healthy individuals with asymptomatic hamstring tightness. Half of study participants received DOS whereas other half received static stretching technique.

Study Overview

Status

Completed

Conditions

Detailed Description

This was a single blind randomized control trial conducted at District Head Quarter teaching hospital Sargodha, Sargodha institute of health sciences Sargodha, Sadiq hospital Sargodha (march 2018-June 2018). Sample size of 83 individuals was calculated through Open Epi tool version 3 with 95 % confidence interval (CI), and power 80%. 83 individuals were screened out on the basis of inclusion and exclusion criteria. Individuals of this selected population were randomly allocated as 42 individuals in Dynamic Oscillatory Stretch(DOS) group and 41 individuals in Static Stretching(SS) group by sealed envelope method.

After the application of hot pack treatment of 7-10 minutes to both groups dynamic oscillatory stretch technique (30 repetitions each of 2 seconds stretch duration in one session) was applied to DOS group and SS stretching (2 repetitions each of 30 seconds in one session) was applied to SS group.

Assessment was done at baseline, immediate post-intervention levels (immediately) and post-intervention level after 1 hour. At baseline and immediately post-intervention level there was no dropout but after 1 hour post-intervention level there were two dropouts from DOS group and 1 dropout from SS group. 40 individuals were analyzed in each DOS and SS group. Data analysis was done through Statistical Package of Social Sciences(SPSS) version 20. Normality of different variables was assessed. Shapiro-Wilk test provided the basis for normality distribution of data.

Study Type

Interventional

Enrollment (Actual)

80

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

    • Punjab
      • Sargodha, Punjab, Pakistan, 40100
        • Sargodha institute of health sciences,DHQ teaching hospital Sargodha

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 38 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Males and females with age limit 20 to 40 years,
  • Active knee extension/90-90 test positive for Screening (With AKE range less than 160 degrees),
  • No known history of hip joint or knee joint disease,
  • No history of recent hamstring strain.

Exclusion Criteria:

  • History of sub-acute and chronic back pain of lumber region and SI joint in past 6 months,
  • Neurological pathology,
  • Patients with some kind of particularly specific pathology (e.g. infection, tumor, osteoporosis, lumbar spine fracture, structural deformity, inflammatory disorder).

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: Group I Experimental Dynamic oscillatory stretch(DOS)
Dynamic oscillatory stretch technique (30 repetitions each of 2 seconds stretch duration in one session) was applied to DOS group.
After the application of hot pack treatment of 7-10 minutes, dynamic oscillatory stretch(DOS) technique (30 repetitions each of 2 seconds stretch duration in one session) was applied to DOS group. An experienced orthopedic manual physical therapist provided these techniques to patients .
Active Comparator: Group II Static Stretching(SS) Group
Static stretching (2 repetitions each of 30 seconds in one session) was applied to SS group.
After the application of hot pack treatment of 7-10 minutes , Static stretching (2 repetitions each of 30 seconds in one session) was applied to SS group. An experienced orthopedic manual physical therapist provided these techniques to patients .

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Active Straight Leg Raise Test(ASLR) Immediate effect
Time Frame: 10 minutes

Changes from baseline Active Straight Leg Raise Test(ASLR) was conducted with the participants in supine lying with both lower limbs initially extended. Then patient actively lifted the leg to be tested at hip joint while stabilizing the leg opposite to that of the testing side by using a stabilization belt. Knee on testing side was essentially sustained in full extension throughout the full testing range. Universal goniometer was used to measure range of motion available at hip joint.

Cut off score for the SLR to indicate hamstring tightness is 80 degrees. Therefore, values of SLR below 80 degrees was considered as hamstring tightness. Assessment was done Immediate after giving intervention(10 minutes).

10 minutes
Active Straight Leg Raise Test(ASLR) 1 hour effects
Time Frame: 1 hour

Changes from Baseline Active Straight Leg Raise Test(ASLR) was conducted with the participants in supine lying with both lower limbs initially extended. Then patient actively lifted the leg to be tested at hip joint while stabilizing the leg opposite to that of the testing side by using a stabilization belt. Knee on testing side was essentially sustained in full extension throughout the full testing range. Universal goniometer was used to measure range of motion available at hip joint.

Cut off score for the SLR to indicate hamstring tightness is 80 degrees. Therefore, values of SLR below 80 degrees was considered as hamstring tightness. Assessment was done after 1 hour of intervention.

1 hour
Active Knee Extension Test (AKE) immediate effect
Time Frame: 10 minutes
Changes from Baseline Active knee extension test (AKE), is used to assess hamstring length. It was performed while the participant was in supine lying and involved leg was in 90 degree hip flexion. then participant was asked to extend the knee. For hamstring tightness cut off score AKE angle is 160°. Therefore normal individuals with angle < 160° were considered as individuals with hamstring tightness.Its reliability is 0.94.Assessment was done Immediate after giving intervention(10 minutes).
10 minutes
Active Knee Extension Test (AKE) 1 hour effects
Time Frame: 1 hour
Changes from Baseline Active knee extension test (AKE), is used to assess hamstring length. It was performed while the participant was in supine lying and involved leg was in 90 degree hip flexion. then participant was asked to extend the knee. For hamstring tightness cut off score AKE angle is 160°. Therefore normal individuals with angle < 160° were considered as individuals with hamstring tightness.Its reliability is 0.94. Assessment was done after 1 hour of intervention.
1 hour
Sit and Reach Test (SRT) Immediate effects
Time Frame: 10 minutes
Changes from Baseline Sit and reach test (SRT) is most commonly employed test to measure hamstring flexibility. This tool is used to measure range of hamstring muscle at knee joint.Each participant was instructed to sits on a couch in long sitting position. participants were seated with elongated legs, with hip flexed to 90 degrees and knees were fully extended and the ankles were in relaxed plantar flexion. A measuring ruler/tape was placed,between the feet with 38 cm score was marked tangent to the sole of the feet. Subjects were asked to reach forward with hands one above the other and palms of the hands facing down, while attempting to touch fingertips to toes or as far beyond on measuring tape while keeping the knees straight. Assessment was done Immediate after giving intervention(10 minutes).
10 minutes
Sit and Reach Test (SRT) 1 hours effects
Time Frame: 1 hour
Changes from Baseline Sit and reach test (SRT) is most commonly employed test to measure hamstring flexibility. This tool is used to measure range of hamstring muscle at knee joint.Each participant was instructed to sits on a couch in long sitting position. participants were seated with elongated legs, with hip flexed to 90 degrees and knees were fully extended and the ankles were in relaxed plantar flexion. A measuring ruler/tape was placed,between the feet with 38 cm score was marked tangent to the sole of the feet. Subjects were asked to reach forward with hands one above the other and palms of the hands facing down, while attempting to touch fingertips to toes or as far beyond on measuring tape while keeping the knees straight. Assessment was done after 1 hour of intervention.
1 hour
Passive Straight Leg Raise Test(PSLR) Immediate effects
Time Frame: 10 minutes

Changes from Baseline PSLR test was conducted with the participants in supine lying with both lower limbs initially extended. Then therapist lifted the leg to be tested at hip joint while stabilizing the leg opposite to that of the testing side by using a stabilization belt. Knee on testing side was essentially sustained in full extension throughout the full testing range. Universal goniometer was used to measure range of motion available at hip joint.

Cut off score for the SLR to indicate hamstring tightness is 80 degrees. Therefore, values of SLR below 80 degrees was considered as hamstring tightness. Assessment was done Immediate after giving intervention(10 minutes).

10 minutes
Passive Straight Leg Raise Test(PSLR) 1 hour effects
Time Frame: 1 hour

Changes from Baseline PSLR test was conducted with the participants in supine lying with both lower limbs initially extended. Then therapist lifted the leg to be tested at hip joint while stabilizing the leg opposite to that of the testing side by using a stabilization belt. Knee on testing side was essentially sustained in full extension throughout the full testing range. Universal goniometer was used to measure range of motion available at hip joint.

Cut off score for the SLR to indicate hamstring tightness is 80 degrees. Therefore, values of SLR below 80 degrees was considered as hamstring tightness. Assessment was done after 1 hour of intervention.

1 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric Pain Rating Scale (NPRS) Immediate effects
Time Frame: 10 minutes
Changes from Baseline Numeric pain scale (NPRS) was used to assess pain intensity. it was used to assess the tolerance ability of individuals for pain produced at the end of passive straight leg raise (PSLR) test.It ranges from 0-10. 0 means No pain and 10 means severe pain. Assessment was done after 10 minutes of intervention.
10 minutes
Numeric Pain Rating Scale NPRS 1 hour effects
Time Frame: 1 hour
Changes from Baseline Numeric pain scale (NPRS) was used to assess pain intensity. it was used to assess the tolerance ability of individuals for pain produced at the end of passive straight leg raise (PSLR) test.It ranges from 0-10. 0 means No pain and 10 means severe pain.Assessment was done after 1 hour of intervention.
1 hour

Collaborators and Investigators

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

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)

March 1, 2018

Primary Completion (Actual)

May 30, 2018

Study Completion (Actual)

June 30, 2018

Study Registration Dates

First Submitted

March 12, 2019

First Submitted That Met QC Criteria

March 19, 2019

First Posted (Actual)

March 21, 2019

Study Record Updates

Last Update Posted (Actual)

August 8, 2019

Last Update Submitted That Met QC Criteria

August 7, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • RiphahIU Kanza Masood

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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