Hypopressive Abdominal Exercise in Postpartum Abdominal Diastasis
NCT ID: NCT04238156
Last Updated: 2020-07-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
15 participants
INTERVENTIONAL
2020-01-20
2020-07-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Hypopressive abdominal exercises have been used for postpartum recovery, for specific pathologies related to pregnancy (low back pain, pelvic floor dysfunction ...) and even for the rehabilitation of spinal pathologies. However, there is a lack of studies that determine its effectiveness and clinical utility.
The aim of the study will be to analyze the effects of Hypopressive abdominal exercises on postpartum abdominal diastasis, the tone of the transverse abdominal muscle and the pelvic floor musculature.
A case series design will be applied, with weekly assessment of the outcomes after the intervention and two months after the intervention.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact of Mobile App-Based Exercises on Rectus Diastasis in Women Undergoing Cesarean Birth
NCT07001046
Abdominal Trunk Function After Surgical Repair of Abdominal Rectus Muscle Diastasis
NCT03623594
Comparison of Overall Function Between Postpartum Women With and Without Diastasis Rectus Abdominis
NCT05709704
Diastasis Recti Abdominis Association With Sacroiliac Joint and Pelvic Floor Dysfunction in Postpartum C-section Women
NCT04519840
Push With Lower Uterine Segment Support
NCT02934516
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Hypopressive abdominal exercises
Hypopressive abdominal exercises will be performed in basic postures (standing, sitting and supine position). In each posture, three slow cost-diaphragmatic respiration will be performed followed by an expiratory apnea and a rib cage opening, during 2 to 10 seconds, and an exhalation of 10 to 30 seconds. Each exercise will be repeated three times.
There will be 3 stages of application throughout the 12 intervention sessions, supervised by a physical therapist:
First stage: To explain the concept of hypopressive respiration and how to perform it.
Second stage: To explain and apply the hypopressive abdominal exercises: 1. Axial auto-elongation (reducing curvatures in the sagittal plane); 2. Cervical auto-elongation (chin toward the neck); 3. Moving forward of gravity axis; 4. Activation of the shoulder girdle (shoulder joint decoaptation); 5. Slight knee flexion; 6. Dorsal ankle flexion.
Third stage: To review and update all the exercises, increasing their intensity.
Hypopressive abdominal exercises
Three sessions per week during four consecutive weeks (Total: 12 sessions). Each session time: 30 minutes.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Hypopressive abdominal exercises
Three sessions per week during four consecutive weeks (Total: 12 sessions). Each session time: 30 minutes.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* abdominal diastasis previously diagnosed
* commitment to perform, at least, 80% of the exercises
* signed informed consent
Exclusion Criteria
* pelvic floor disorders before childbirth
* drugs with effects on continence or functional properties of the pelvic floor muscles
* treatment for abdominal diastasis in the last 6 months
* systemic disease that impairs pelvic floor physiology and urination
* menopause
* contraindications to the practice of physical exercise and physical therapy
30 Years
50 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Universidad de Córdoba
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Francisco Alburquerque-Sendín
Ph D, Associate Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Daiana Priscila Rodrigues-de-Souza, PhD
Role: STUDY_DIRECTOR
Universidad de Córdoba
Miriam Ramírez Jiménez, Phys Ther
Role: PRINCIPAL_INVESTIGATOR
Universidad de Córdoba
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Córdoba
Córdoba, , Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
HipoDiastasis4073-2018
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.