Comparison of MET vs Mobilization in Management of Post-partum Backache in Females (NVD) and Cesarean Section Delivery

Sponsor
Superior University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05873114
Collaborator
(none)
50
1
2
5
10

Study Details

Study Description

Brief Summary

Effectiveness Comparison of Effects of Muscle Energy Technique (MET) vs Mobilization in Management of Post-partum Backache in Females With Normal Vaginal Delivery (NVD) and Cesarean Section Delivery

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Mobilization
  • Diagnostic Test: Muscle Energy Technique (MET)
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Comparison of Effects of Muscle Energy Technique (MET) vs Mobilization in Management of Post-partum Backache in Females With Normal Vaginal Delivery (NVD) and Cesarean Section Delivery
Actual Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Muscle Energy Technique (MET)

Diagnostic Test: Muscle Energy Technique (MET)
Effects of Muscle Energy Technique (MET) in Management of Post-partum Backache in Females With Normal Vaginal Delivery (NVD) and Cesarean Section Delivery

Other: Mobilization

Diagnostic Test: Mobilization
Effects of Mobilization in Management of Post-partum Backache in Females With Normal Vaginal Delivery (NVD) and Cesarean Section Delivery

Outcome Measures

Primary Outcome Measures

  1. NPSR [6 Months]

    Numeric pain rating scale

  2. Owestry [6 Months]

    Owestry low back pain disability questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects with age group 20 to 40 year.

  • low back pain and disability after normal vaginal delivery or c-section delivery will be included.

Exclusion Criteria:
  • Subjects who had neurological deficit.

  • spinal tumors, scoliosis

  • underwent spinal surgery

  • prolapsed intervertebral disc with or without radiculopathy will be excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chaudary Muhammad Akram Teaching Hospital, Azra Naheed Medical College, Superior University Lahore Punjab Pakistan

Sponsors and Collaborators

  • Superior University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Muhammad Naveed Babur, Principal Investigator, Superior University
ClinicalTrials.gov Identifier:
NCT05873114
Other Study ID Numbers:
  • DPT/Batch-Fall18/540
First Posted:
May 24, 2023
Last Update Posted:
May 24, 2023
Last Verified:
May 1, 2023
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 24, 2023