Gluteal Activation With or Without Traction Straight Leg Raise Technique

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04757415
Collaborator
(none)
38
1
2
9.5
4

Study Details

Study Description

Brief Summary

This study was a Randomized clinical trial conducted to determine the Effects of gluteal activation with or without traction straight leg raise technique among patients of sacroiliac joint syndrome so that in future this study will be helpful for other clinician to determine that how much gluteal activation is important in low back pain or sacroiliac joint syndrome, and how it affects our sling system.

Condition or Disease Intervention/Treatment Phase
  • Other: Traction straight leg raise technique for hamstring
  • Other: Gluteal activation exercises,Hotpack
N/A

Detailed Description

Non Probability Convenient sampling was done . Patients following eligibility criteria from Sports and Spine Professionals ,Lahore were considered. Sample size was calculated with Epi tool calculator. 38 Participants were randomly allocated in two groups equally via convenient sampling method. Baseline assessment was done initially. Group A was given gluteal activation exercises with traction straight leg raise technique for hamstring and Group B was gluteal activation exercises without traction straight leg raise technique for hamstring. Duration of research was almost 6 months. Patient will undergo 10 treatments in five weeks. Each session will take 30 minutes. Pre and Post treatment readings were taken in 1st and 10th session over a 5 week period respectively. Assessment was done via sphygmomanometer and numeric pain rating scale for assessing muscle strength of gluteus maximum and pain levels respectively. All participants were provided written informed consent prior to commencement of the procedures. They were free to quit the treatment at any stage of research. Data was analyzed by using SPSS version 23.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
38 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Masking Description:
single
Primary Purpose:
Treatment
Official Title:
Effects of Gluteal Activation With or Without Traction Straight Leg Raise Technique Among Patients of Sacroiliac Joint Syndrome
Actual Study Start Date :
Oct 15, 2021
Anticipated Primary Completion Date :
Jul 31, 2022
Anticipated Study Completion Date :
Jul 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Traction straight leg raise technique for hamstring.

Experimental group underwent conventional physiotherapy treatment (hot pack) followed by five main gluteal activation exercises three in first five sessions and rest two in remaining five sessions along with traction straight leg raise technique. Each session took 30 minutes . Participants were treated 10 times over a 5 week period with 2 treatment sessions per week. Pre and Post treatment readings were taken in 1st and 10th session over a 5 week period respectively. Assessment was done via Numeric pain rating scale and sphygmomanometer for assessing pain intensity and muscle strength of gluteus maximus.

Other: Traction straight leg raise technique for hamstring
traction straight leg raise technique is used along with gluteal exercises

Experimental: Gluteal activation exercises

Experimental group underwent conventional physiotherapy treatment (hot pack) followed by five main gluteal activation exercises three in first five sessions and rest two in remaining five sessions. Each session took 30 minutes . Participants were treated 10 times over a 5 week period with 2 treatment sessions per week. Pre and Post treatment readings were taken in 1st and 10th session over a 5 week period respectively. Assessment was done via Numeric pain rating scale and sphygmomanometer for assessing pain intensity and muscle strength of gluteus maximus.

Other: Gluteal activation exercises,Hotpack
only gluteal activation exercises were performed without traction straight leg raise technique

Outcome Measures

Primary Outcome Measures

  1. Change of muscle strength of gluteus maximum by "Sphygmomanometer" [Baseline at 1st session on 1st week,at 10th sessions on 5th week]

    change in strength of gluteal muscle was checked at 1st session and then follow up at end of 10th session

Secondary Outcome Measures

  1. change in pain by "Numeric Pain rating Scale" [Baseline at 1st session on 1st week , at 10th session on 5th week]

    change in pain intensity was checked at 1st session and then follow up at end of 10th session

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 60 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Subjects with LBP below the level of L5,

  2. With pain over the posterior aspect of SI joint around posterior superior iliac spine and buttock with or without above knee leg pain.

  3. Females only

Exclusion Criteria:
  1. Had radicular pain with neurological (sensory or motor) deficits,

  2. Had a history of spinal surgery, spinal, pelvic, or lower extremity fracture; hospitalization for trauma or motor vehicle accident;

  3. Hip or knee dysfunctions;

  4. Pregnancy;

  5. Any systemic disease such as arthritis, tuberculosis, liver, or kidney failure

  6. Subjects with leg length discrepancies, because of its potential effect on hamstring muscle length were also excluded. -

Contacts and Locations

Locations

Site City State Country Postal Code
1 Riphah IU Lahore Pakistan 54000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Rabiya Noor, PhD, Riphah International University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT04757415
Other Study ID Numbers:
  • REC/LHR/20/0103 Farzana Saqib
First Posted:
Feb 17, 2021
Last Update Posted:
Jul 15, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 15, 2022