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Clinical Trials in Poland / NCT07839572
Recruiting Not applicable

Risk Factors and Exercise Effects on Abdominal Separation in Seniors

NCT07839572 · tracked via the Priya Life Science Poland tracker
Phase
Not applicable
Started
2026-08-17
Last updated
2026-09-24

Condition(s) studied

Diastasis Recti Abdominis (DRA)Aging

Investigational drug(s) / intervention(s)

Abdominal Exercise Program

Abdominal Exercise Program: An 8-to-10-week exercise program designed for older adults diagnosed with diastasis recti abdominis. The intervention includes targeted abdominal muscle activation and trunk stabilization exercises aimed at reducing inter-recti distance (IRD) and improving linea alba stability.

Study summary

This study aims to evaluate the prevalence of diastasis recti abdominis (DRA) in the geriatric population and assess the effectiveness of a targeted exercise program on inter-recti distance (IRD) and linea alba stability. Diastasis recti abdominis is a common condition characterized by the separation of the rectus abdominis muscles, which can affect trunk stability, posture, and pelvic floor function. While heavily researched in postpartum women, data regarding DRA in older adults remains limited. In the first observational phase, 500 participants aged 60 and older will undergo ultrasonographic (USG) measurement of the inter-recti distance (2 cm above and 2 cm below the umbilicus) and an assessment of linea alba stability during active movements (cervical flexion, leg raise, and trunk extension). Abdominal circumference will also be measured. Risk factors, functional status, physical activity, urinary incontinence, and low back pain will be evaluated using standardized questionnaires (IPAQ, ICIQ-UI SF, Revised Oswestry Low Back Pain Disability Index) and a custom survey. Participants diagnosed with DRA (IRD 2 cm and/or linea alba instability) will be invited to join the second, interventional phase. They will be randomly allocated to either an experimental exercise group or a control group. The exercise group will perform a structured 8-to-10-week exercise program, while the control group receives no intervention. Follow-up assessments (USG, stability testing, and questionnaires) will be conducted for both groups after the 8-10 week period to compare outcomes.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Men and women aged 60 years and older (≥ 60 years of age). * Provision of signed informed consent to participate in the study. Exclusion Criteria: * Inability to communicate effectively in Polish. * Inability to perform cervical spine flexion. * Lack of written informed consent to participate in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Medical University of Gdańsk, Department of Clinical Physiotherapy Gdansk Pomeranian Recruiting

More Medical University of Gdansk trials in Poland

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07839572 on ClinicalTrials.gov ↗ ← All trials in Poland