Actively Recruiting
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
Eligibility Criteria
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
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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) at week 36 of pregnancy
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
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
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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