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 |
---|---|---|
|
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
- NPSR [6 Months]
Numeric pain rating scale
- 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: