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Static and Dynamic Core Stability Exercises in Potpartum Back Pain

Primary Purpose

Back Pain

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Static exercises
Dynamic exercises
Sponsored by
Riphah International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Back Pain focused on measuring Pain and disability in postpartum

Eligibility Criteria

18 Years - 35 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age groups of 18 to 35
  • Pain more than 4/10 on VAS
  • Without referred pain to lower limbs
  • Women with normal delivery

Exclusion Criteria:

  • Nulliparous women
  • Osteoporosis and OA
  • Systemic arterial hypertension
  • Hypersensitivity to electrical modalities
  • Any fracture (spine, rib) or injury
  • Any abdominal surgery
  • Any other general ailment
  • Vertebral or disc pathologies

Sites / Locations

  • General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Static exercises

Dynamic exercises

Arm Description

static exercises i.e traditional exercises along with base line treatment of TENS and hot pack

dynamic (Swiss ball) exercises along with base line treatment of TENS and hot pack

Outcomes

Primary Outcome Measures

Oswestry disability index
Oswestry disability index (ODI) is used to measure disability. A score of 0-20 reflects minimal disability, 21-40 moderate disability, 41-60 severe disability, 61-80 crippled, and 81-100 bed-bound.
visual analog scale
Visual analog scale (VAS) is usd to measure pain intensity. The findings suggested that 100-mm VAS ratings of 0 to 4 mm can be considered no pain; 5 to 44 mm, mild pain; 45 to 74 mm, moderate pain; and 75 to 100 mm, severe pain.

Secondary Outcome Measures

Full Information

First Posted
February 20, 2022
Last Updated
April 15, 2022
Sponsor
Riphah International University
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1. Study Identification

Unique Protocol Identification Number
NCT05342181
Brief Title
Static and Dynamic Core Stability Exercises in Potpartum Back Pain
Official Title
Comparison of Static and Dynamic Core Stability Exercises on Pain and Disability in Postpartum Back Pain
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
September 21, 2021 (Actual)
Primary Completion Date
October 25, 2021 (Actual)
Study Completion Date
November 14, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Riphah International University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To compare the effects of static exercises with dynamic core stability on pain and disability in postpartum back pain.
Detailed Description
The study comprised 28 participants. The individuals were subdivided into binary groups, group A performed static exercises and group B performed dynamic exercises including swiss ball, each containing 14 subjects. Baseline treatment (Hot pack, TENS and posture correction) to both groups was given along with core stability exercises. Core stability exercises were performed on both group for 4 weeks. The pretreatment and post treatment tests are measured using the scale VAS (visual analog scale) and Oswestry disability index questionnaire. Both groups have shown the improvement in postpartum lumber pain and an improved in daily life activities. But swiss ball exercises have more significant improvement on pain and disability in patients having postpartum lumber pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Back Pain
Keywords
Pain and disability in postpartum

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Static exercises
Arm Type
Experimental
Arm Description
static exercises i.e traditional exercises along with base line treatment of TENS and hot pack
Arm Title
Dynamic exercises
Arm Type
Experimental
Arm Description
dynamic (Swiss ball) exercises along with base line treatment of TENS and hot pack
Intervention Type
Other
Intervention Name(s)
Static exercises
Intervention Description
Participants will be treated with static core muscle exercises that are traditional group of exercises : supine bridge plank oblique crunch side lying with Abduction This program includes static exercises performed thrice a week for 4 weeks.This exercise comprises 5 minutes warm up and slight stretching.Rest time of 2-3 minutes with proper stretching in between sets of activity. Subjects will be requested to undertake cool down exercises, which include aerobic workouts followed by stretching exercises, at the end of each day's exercise programme. Before beginning the next session's training, the subjects will be asked if they had any discomfort.
Intervention Type
Other
Intervention Name(s)
Dynamic exercises
Intervention Description
Participants will be treated with dynamic core muscle exercises that were swiss ball exercises bridging straight leg raise in prone lying straight leg raise with hand raise in prone lying pelvic tilts This program includes static exercises performed thrice a week for 4 weeks.This exercise comprises 5 minutes warm up and slight stretching.Rest time of 2-3 minutes with proper stretching in between sets of activity. Subjects will be requested to undertake cool down exercises, which include aerobic workouts followed by stretching exercises, at the end of each day's exercise programme. Before beginning the next session's training, the subjects will be asked if they had any discomfort.
Primary Outcome Measure Information:
Title
Oswestry disability index
Description
Oswestry disability index (ODI) is used to measure disability. A score of 0-20 reflects minimal disability, 21-40 moderate disability, 41-60 severe disability, 61-80 crippled, and 81-100 bed-bound.
Time Frame
4th week
Title
visual analog scale
Description
Visual analog scale (VAS) is usd to measure pain intensity. The findings suggested that 100-mm VAS ratings of 0 to 4 mm can be considered no pain; 5 to 44 mm, mild pain; 45 to 74 mm, moderate pain; and 75 to 100 mm, severe pain.
Time Frame
4th week

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Age groups of 18 to 35 Without referred pain to lower limbs Women with normal delivery
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age groups of 18 to 35 Pain more than 4/10 on VAS Without referred pain to lower limbs Women with normal delivery Exclusion Criteria: Nulliparous women Osteoporosis and OA Systemic arterial hypertension Hypersensitivity to electrical modalities Any fracture (spine, rib) or injury Any abdominal surgery Any other general ailment Vertebral or disc pathologies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sara Aabroo, pp-dpt
Organizational Affiliation
General hospital lahore
Official's Role
Principal Investigator
Facility Information:
Facility Name
General Hospital
City
Lahore
State/Province
Punjab
ZIP/Postal Code
54000
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
No

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Static and Dynamic Core Stability Exercises in Potpartum Back Pain

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