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Clinical Trials/NCT05397899
NCT05397899CompletedNot Applicable

Effects of Abdominal Hypopressive Technique on Postpartum Low Back Pain

Riphah International University1 site in 1 country31 target enrollmentStarted: June 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
31
Locations
1
Primary Endpoint
Maternal Postpartum Quality of Life Index

Study Overview

Brief Summary

Postpartum Low back pain (PP-LBP) is more common and can lead to limitations to women's daily activity. Pregnancy related low back pain has been reported to occur in 55% to 78% women worldwide.This study is planned to determine the effects of abdominal hypopressive technique on postpartum low back pain, mobility and disability.

Detailed Description

literature suggests the use of hypopressive abdominal techniques to be effective in increasing the thickness of the abdominal muscles and hence add to the stability of the spine and alleviation of low back pain in the postpartum period. This will be a randomized controlled trial, with two groups.

Participants in the experimental group will learn how to perform the "hypopressive maneuver", which consisted of exhaling to their expiratory reserve volume, then holding their breath (apnea), and expanding their rib cage, to draw their abdominal wall inward and cranially without inhalation. control group will perform general exercises. Both groups will be assessed at pre and post test (after 6weeks)

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

outcome assessor will be kept blind about the group of patients and treatment received.

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Postpartum non-radiating low back Pain
  • •LBP severity >3 on numeric pain rating scale (NPRS)
  • •Spontaneous vaginal delivery

Exclusion Criteria

  • •Prenatal history of low back pain
  • •Caesarean section
  • •Hypertension
  • •Puerperium period
  • •Arterial complications
  • •Neurological deficit
  • •Disc Bulge
  • •Lumbar Radiculopathy

Arms & Interventions

AHT group

Experimental

This group will receive Abdominal hypopressive exercises. Each AHT will be repeated 3-5 times with 1 min rest between exercises (shift to new posture, lying,sitting and standing). Between 6 and 15 hypopressive exercises (HEs) will be performed within each session based on the participant's mastery of the exercises and readiness to progress, for 6 weeks.

Intervention: Abdominal hypopressive Exercises (AHE) (Other)

General exercise group

Active Comparator

This group will receive general exercises (Bridging, knee to chest, Straight leg rise) these will be repeated 3-5 times with 1 min rest between exercises. Between 6 and 15 repetitions will be performed within each session based on the participant's mastery of the exercises and readiness to progress. Each exercise to be repeated 3-5 times per set, and participants will be asked to perform technique once daily for 6 weeks

Intervention: General exercises (Other)

Outcomes

Primary Outcomes

Maternal Postpartum Quality of Life Index

Time Frame: Changes from Baseline to 6th week

It is a sixteen-item scale, which is a valid and reliable instrument for postpartum QOL assessment. It includes items on the different aspects of postpartum QOL and can be used for the early diagnosis of impaired postpartum QOL. The QoL score ranges from 0 to 30, with higher scores indicating higher QoL.

Pregnancy Mobility Index

Time Frame: Changes from Baseline to 6th week

It is self-report mobility scale designed specifically for the pregnant women. The internal consistency (Cronbach's alpha) is 0.8 or higher indicating a good construct validity. The assumptions that the Pregnancy Mobility Index scores increase during pregnancy and decrease after delivery and that women with back or pelvic problems scored higher on the Pregnancy Mobility Index domains than women without back or pelvic pain were confirmed, indicating a good criterion validation. Its scores range from 0 to 100, in which 0 equals 'normal performance' and 100 indicates 'maximum disability

Numeric Pain Rating Scale (NPRS)

Time Frame: Changes from Baseline to 6th week

The pain score was assessed using the numeric pain rating scale (NPRS) is a scoring system, wherein the pain level was quantified on a scale of 0 (no pain) to 10 (worst possible pain). The NPRS is a valid and frequently employed method of musculoskeletal pain assessment.

Secondary Outcomes

  • Oswestry Low Back Pain Disability Index(ODI)(Changes from Baseline to 6th week)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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