Risk Factors and Exercise Effects on Abdominal Separation in Seniors
Risk Factors and the Impact of a Physical Exercise Program on Inter-Recti Distance in the Geriatric Population
- Diastasis Recti Abdominis (DRA)
- Aging
At a glance
- Phase
- Phase not stated
- Study type
- Interventional
- Sponsor
- Medical University of Gdansk
- Enrolment target
- 500
- Started
- 17 August 2026
- Main results due
- 31 July 2029
- Study sites
- 1
- Registry updated
- 24 September 2026
Can you take part?
- Aged 60 years and over.
- Open to any sex.
- Healthy volunteers can take part.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
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.
What this study is about
In the sponsor’s own words, from the registry.
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.
Study sites(1)
Medical University of Gdańsk, Department of Clinical Physiotherapy
Gdansk, Pomeranian, Poland
Recruiting
Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07839572. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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