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
About this trial
This is an interventional treatment trial for Back Pain focused on measuring Pain and disability in postpartum
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
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
NCT ID
NCT05342181
First Posted
February 20, 2022
Last Updated
April 15, 2022
Sponsor
Riphah International University
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
Learn more about this trial
Static and Dynamic Core Stability Exercises in Potpartum Back Pain
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