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Clinical Trials/NCT07037368
NCT07037368
Active, not recruiting
Not Applicable

Impact of Delivery Mode on Coccydynia, Pelvic Girdle Pain and Rectus Diastasis in Postpartum Females: a Comparative Study

Superior University1 site in 1 country73 target enrollmentStarted: March 4, 2025Last updated:

Overview

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
73
Locations
1
Primary Endpoint
Visual Analog Scale

Overview

Brief Summary

This comparative observational study investigates the impact of delivery mode vaginal delivery versus cesarean section on the prevalence and severity of three postpartum musculoskeletal complications: coccydynia, pelvic girdle pain (PGP), and rectus diastasis (RD). Conducted on postpartum females aged 20-40 years within 6 weeks to 6 months after childbirth, the study aims to highlight musculoskeletal outcomes often overlooked in standard postpartum care.

Detailed Description

A total of 73 participants were selected through non-probability sampling from rehabilitation centers and home-based postpartum populations in Lahore. Pain intensity and musculoskeletal impairments were assessed using validated tools: the Visual Analog Scale (VAS) for coccydynia, Pelvic Girdle Questionnaire (PGQ) for PGP, and finger-width palpation technique for RD. The data collection involved both self-reported questionnaires and clinical assessments by trained professionals. The goal is to identify how delivery mode influences musculoskeletal health and to support the development of more tailored physiotherapy interventions and postpartum care strategies.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

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

Inclusion Criteria

  • Postpartum females aged 20-40 years
  • Females who delivered via vaginal delivery or cesarean section
  • 6 weeks to 6 months postpartum period
  • Willingness to participate and provide informed consent

Exclusion Criteria

  • Females with a history of pelvic or spinal surgery prior to pregnancy
  • Known cases of pre-existing musculoskeletal disorders (e.g., scoliosis, chronic back pain)
  • Multiple pregnancies (twins or more) in the current or previous delivery
  • Postpartum complications unrelated to delivery mode (e.g., sepsis, trauma)

Outcomes

Primary Outcomes

Visual Analog Scale

Time Frame: 6 Month

A 10 cm horizontal line marked from 0 (no pain) to 10 (worst imaginable pain). Scoring: The participant marks a point on the line that best represents their pain intensity. The score is measured in centimeters from the "no pain" end. Higher scores indicate more severe pain.

Pelvic Girdle Questionnaire (PGQ)

Time Frame: 6 Months

Contains 25 items divided into two domains: activity limitations (20 items) and symptoms (5 items). Scoring: Each item is rated on a 4-point scale (0 = not at all, 1 = to a small extent, 2 = to some extent, 3 = to a great extent). Scores are summed, converted into a percentage of the maximum possible score. Higher percentages reflect greater pelvic girdle pain and disability.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Naveed Babur

Principal Investigator

Superior University

Study Sites (1)

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