Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
ID07430865

The RECOVER Study - Recovery of Pelvic Floor Structure and Function After Vaginal Childbirth- a Longitudinal Cohort Study With an Embedded Pilot Trial

Led by Vastra Gotaland Region · Updated on 2026-05-27

380

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how the pelvic floor recovers during the first year after vaginal childbirth and whether early, personalized pelvic floor muscle training can improve recovery and reduce symptoms in people who experience pelvic floor issues after delivery. The study focuses on changes in pelvic floor muscles and surrounding tissues, and their relationship to urinary, bowel, and vaginal symptoms. It includes an observational cohort and a pilot randomized trial to compare early training with standard postpartum care. Participants receive either early individualized pelvic floor muscle training starting 2-3 weeks after childbirth or standard postpartum care. The training involves progressive exercises with 8-10 maximal contractions held for 6-8 seconds, done 2-3 times daily for at least 12 weeks. Participants also receive education, exercise diaries, and digital follow-ups. Ultrasound and clinical assessments evaluate pelvic floor structure and function at multiple time points. Participants attend clinic visits at 6 weeks and 6 months postpartum for ultrasound and clinical assessments, and complete questionnaires about symptoms, physical activity, and quality of life at 6 weeks, 4, 6, and 12 months. Researchers measure urinary, vaginal, and bowel symptoms, pelvic floor muscle strength and tone, and anatomical changes using ultrasound. The study also tracks adherence to training and improvement perceptions to understand pelvic floor recovery and the impact of early rehabilitation over 12 months.

CONDITIONS

Brief Title

The RECOVER Study - Postpartum Recovery of Pelvic Floor Structures and the Impact of Early Rehabilitation

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals over 18 years old who delivered a single child vaginally between 37 and 41 weeks of gestation
  • Birthweight of the child at least 2500 grams
Not Eligible

You will not qualify if you...

  • Delivered via cesarean section
  • Multiparous with previous third- or fourth-degree tears
  • History of major urogynecological surgery
  • Known neurological disorder affecting assessment outcomes (e.g., stroke, multiple sclerosis)
  • Severe connective tissue disorders affecting assessment outcomes
  • New pregnancy over 6 weeks during the study period
  • Pain with vaginal penetration, tampon use, or gynecological exams preventing participation
  • Visible wound complications assessed by REEDA excluding from first ultrasound and vaginal palpation

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) at week 36 of pregnancy

Monitoring

Duration - 12 months postpartum

Participants are followed over 12 months postpartum with assessments to observe pelvic floor recovery and symptoms.

Visits at 6 weeks, 2 weeks (for some assessments), 4 months, 6 months, and 12 months postpartum

Outpatient Treatment

Duration - At least 12 weeks starting 2-3 weeks postpartum

Participants randomized to early individualized pelvic floor muscle training receive physiotherapy starting 2-3 weeks after delivery, including exercise guidance and follow-up visits.

Digital follow-ups every second week for 3 months, then every fourth week; additional in-person physiotherapy visits as needed

Trial Site Locations

Total: 2 locations

1

Sahlgrenska hospital, Östra

Gothenburg, Sweden, 43541

Actively Recruiting

2

University of Gothenburg

Gothenburg, Sweden

Actively Recruiting

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Research Team

S

Sabine Vesting, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Frequently Asked Questions

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