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

Active, not recruiting

• Conditions: Pelvic Girdle Pain; Rectus Diastasis

• Registration Number: NCT07037368
• Lead Sponsor: Superior University

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 Timeline

• Study Start: 2025-03-04
• Status Verified: 2025-06
• Primary Completion: 2025-06-01
• Study First Submitted: 2025-06-17
• Study First Submitted QC: 2025-06-17
• Last Update Submitted: 2025-06-17
• Study First Posted: 2025-06-25
• Last Update Posted: 2025-06-25
• Study Completion: 2025-09-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: Female
• Target Recruitment: 73

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)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Visual Analog Scale	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)	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.

Trial Locations

Locations (1)

Superior University CRC; 🇵🇰 Lahore, Punjab, Pakistan