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Static and Dynamic Core Stability Exercises in Potpartum Back Pain

Comparison of Static and Dynamic Core Stability Exercises on Pain and Disability in Postpartum Back Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05342181
Enrollment
31
Registered
2022-04-22
Start date
2021-09-21
Completion date
2021-11-14
Last updated
2022-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Back Pain

Keywords

Pain and disability in postpartum

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.

Interventions

OTHERStatic exercises

Participants will be treated with static core muscle exercises that are traditional group of exercises : 1. supine bridge 2. plank 3. oblique crunch 4. 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.

Participants will be treated with dynamic core muscle exercises that were swiss ball exercises 1. bridging 2. straight leg raise in prone lying 3. straight leg raise with hand raise in prone lying 4. 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.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Oswestry disability index4th weekOswestry 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 scale4th weekVisual 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.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026