Muscle Energy Technique on Sacroiliac Dysfunction

Sponsor
Cairo University (Other)
Overall Status
Completed
CT.gov ID
NCT05088837
Collaborator
(none)
40
1
2
5.9
6.8

Study Details

Study Description

Brief Summary

Sacroiliac pain is a huge problem in women during pregnancy and postpartum period. Muscle energy technique has potential effect in decreasing the pain and disability

Condition or Disease Intervention/Treatment Phase
  • Other: muscle energy technique
  • Other: ice and heat packs
N/A

Detailed Description

A sample of forty women diagnosed with postpartum sacroiliac dysfunction, their ages ranged from 20 to 40 years and their BMI was ranged from 25-30 kg / m2 participated in this study, they were selected and divided randomly into 2 equal groups (A&B). Group (A) (Control group): consisted of 20 patients, they received muscle energy technique for 12 sessions, 3 sessions / week. Group (B) (Study group): consisted of 20 patients, they received alternative heat and ice for another 20 minutes /session (10 minutes for each). All patients in both group were evaluated at the beginning of the study and after 12 sessions through measuring pain intensity using visual analog scale and disability using oswestry disability index (ODI)

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Group (A) (Control group): consisted of 20 patients, they received muscle energy technique for 12 sessions, 3 sessions / week. Group (B) (Study group): consisted of 20 patients, they received alternative heat and ice for another 20 minutes /session (10 minutes for each).Group (A) (Control group): consisted of 20 patients, they received muscle energy technique for 12 sessions, 3 sessions / week. Group (B) (Study group): consisted of 20 patients, they received alternative heat and ice for another 20 minutes /session (10 minutes for each).
Masking:
Single (Outcomes Assessor)
Masking Description:
An independent individual randomly appointed to all participants to either group (A) (n=20) or group (B) (n=20) by numbers that were picked from the closed envelopes.
Primary Purpose:
Treatment
Official Title:
Effect of Muscle Energy Technique on Postpartum Sacroiliac Joint Dysfunction
Actual Study Start Date :
Feb 1, 2020
Actual Primary Completion Date :
Jun 30, 2020
Actual Study Completion Date :
Jul 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: muscle energy technique

muscle energy technique was performed in the form of post-isometric relaxation technique for iliopsoas, hamstrings, and erector spinae and quadratus lumborum muscles, it was done 3 times per session for 12 sessions.

Other: muscle energy technique
MET was performed in the form of post-isometric relaxation technique for iliopsoas, hamstrings, and erector spinae and quadratus lumborum muscles. the limb was taken very slightly beyond the restriction barrier and was held there for 10-30 seconds, it was done 3 times per session for 12 sessions.

Experimental: ice and heat packs

Alternating ice and heat (20 min , 10 heat,10 cold),3times per week for 12sessions.

Other: ice and heat packs
Applying 20 minutes: 10 minutes hot,10 minutes cold on sacroiliac area, 3 times per week for 12 sessions

Outcome Measures

Primary Outcome Measures

  1. visual analog scale Visual anlage scale [4 weeks]

    It was used for determining pain intensity before and after the treatment course for each patients in both groups (A&B). Visual analogue scale is a-10 centimeters line, at one end was written (no pain = zero) and at the other end was written (worst pain the patient ever felt = 10)

Secondary Outcome Measures

  1. Oswestry disability index [4 weeks]

    The self-completed questionnaire contains ten topics concerning intensity of pain, lifting, ability to care for oneself, ability to walk, ability to sit, sexual function, ability to stand, social life, sleep quality, and Each question is scored on a scale of 0-5 with the first statement being zero and indicating the least amount of disability and the last statement is scored 5 indicating most severe disability. The scores for all questions answered are summed, were used to measure the level of disability before and after treatment

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Their ages ranged from 20 to 40 years .

  • Their BMI was ranged from 25-30 kg / m2

Exclusion Criteria:
  • hip fracture,

  • SIJ infection.

  • scoliosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ghada Ebrahim Elrefaye Giza Egypt 12613

Sponsors and Collaborators

  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ghada Ebrahim El Refaye, assistant professor Department of Physical Therapy for Women's Health, Faculty of Physical therapy, Cairo University, Egypt, Cairo University
ClinicalTrials.gov Identifier:
NCT05088837
Other Study ID Numbers:
  • Cairo Un113
First Posted:
Oct 22, 2021
Last Update Posted:
Oct 22, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ghada Ebrahim El Refaye, assistant professor Department of Physical Therapy for Women's Health, Faculty of Physical therapy, Cairo University, Egypt, Cairo University

Study Results

No Results Posted as of Oct 22, 2021