pelvic floor dysfunction, diastasis recti abdominis, lumbopelvic pain, and impairment of core muscle groups and physical function
Conditions
Interventions
Control Group (CG): Standardized Routine Exercise-Rehabilitation Guidance Group:Standardized Routine Exercise-Rehabilitation Guidance
Intervention Group (IG): Precision Exercise-Prescription Rehabilitation Pathway Group:Precision Exercise-Prescription Rehabilitation Pathway Intervention for Postpartum Women
Sponsors
The Third Affiliated Hospital Of Henan Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1.Female participants aged 18–45 years, 6 weeks to 1 year postpartum, with stable vital signs and deemed suitable for study-related assessments and exercise-based rehabilitation intervention. 2.Participants with a clear need for postpartum rehabilitation based on standardized assessments, meeting at least one of the following conditions: reduced pelvic floor muscle function, diastasis recti abdominis, persistent pain, functional limitation of the pelvic girdle, or abnormal findings from functional or symptom-based assessments. 3.Participants who are able to understand the study purpose, procedures, and potential risks, and are willing to complete baseline assessments, interventions, and follow-up observations. 4.Participants who voluntarily agree to participate in the study and provide written informed consent.
Exclusion criteria
Exclusion criteria: 1.Participants meeting any of the following conditions will be excluded from this study:; 2.Acute postpartum complications, active infection, significant bleeding, or any other condition deemed by the study physician to be currently unsuitable for exercise intervention. 3.Severe organic diseases involving major organs, such as the heart, lungs, liver, or kidneys, or other serious underlying diseases that may affect exercise safety or the evaluation of study outcomes. 4.Severe pelvic floor, abdominal wall, pelvic, or spinal disorders, or markedly unstable symptoms for which exercise intervention may aggravate the condition. 5.Current receipt of other systematic rehabilitation treatments that may affect the evaluation of study outcomes, or current participation in another clinical study. 6.Severe cognitive, psychiatric, or communication disorders that prevent understanding of the study content or cooperation with assessments, intervention, and follow-up. 7.Refusal to provide written informed consent, or withdrawal of informed consent during the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Diastasis recti abdominis;Pelvic floor muscle function; | — |
Secondary
| Measure | Time frame |
|---|---|
| Sleep quality;Pelvic floor symptom burden;Body weight and body mass index;Laboratory safety tests;Blood pressure and heart rate;Maternal role identity / parental identity development;Quality of life;Pain intensity;Psychological status;Early safety and adherence follow-up;Pelvic girdle function;Pelvic floor ultrasound or pelvic floor electrophysiological assessment;Adverse events, serious adverse events; | — |
Countries
China
Contacts
Public ContactMeng Jie
The Third Affiliated Hospital Of Henan Medical University
Outcome results
None listed