Community Physical Exercise Program in Chronic Disease
- NCT ID
- NCT06771024
- Registry status
- Not yet recruiting
- Study type
- Not specified in the registry data
- Phase
- Not applicable
- Sponsor
- Associação para o Desenvolvimento do Centro Académico de Investigação e Formação Biomédica do Algarv
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Enrollment: 150 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* Adults aged ≥50 years;
* At least 2 of the following: Prior cardiovascular disease (\>12 months); High cardiovascular risk (SCORE2 or SCORE2 O.P.); Post-stroke (ischemic or hemorrhagic) with treated etiology; Type 2 Diabetes (\> 6 months, ADA); Osteoarthristis (clinical signs/symptoms, NICE); Overweight/Obesity (BMI ≥ 27 kg/m2).
* Autonomous walking.
* Able to provide informed consent.
* Stable medications for ≥ 3 months (related to diagnoses of interest).
* Physical activity below WHO recommendations.
* No contraindications to exercise (cardiovascular, cerebrovascular, respiratory, musculoskeletal) according to ACSS.
Exclusion Criteria:
* Moderate to severe cognitive impairment - Montreal Cognitive Assessment (MoCA).
* Type 2 Myocardial Infarction.
* Class III or IV angina (Canadian Cardiovascular Society).
* Class III or IV angina (New York Heart Association).
* Uncontrolled CVD: symptomatic arrhythmias with hemodynamic compromise; severe symptomatic aortic valve stenosis; uncontrolled symptomatic heart failure; endocarditis, pericarditis, or active myocarditis; acute aortic syndrome; suspected or known dissecting aneurysm; acute systemic infections.
* Pacemaker user.
* Neurological disorders affecting gait.
* Severe diabetes-related complications contraindicating exercise (poor metabolic control, diabetic foot, diabetic retinopathy, diabetic nephropathy, and diabetic autonomic neuropathy).
* Recent use of insulin or sulphonylureas (\< 3 months).
* Untreated stroke etiology: indication for revascularization; non-anticoagulated atrial fibrillation; intracranial atherosclerotic occlusive disease.
* Musculoskeletal or ocular conditions preventing strength training (acute herniated disc, fractures, recent spinal surgery, glaucoma with elevated intraocular pressure).
* Terminal illness.
* Inability to understand basic oral or written Portuguese.
* Participation in supervised dietary intervention.
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Portugal
- Algarve, Portugal: 1
Sample of listed locations
- Algarve Biomedical Center — Faro, Algarve, 8005-139, Portugal — Site recruitment status not specified in the registry data
Study details
- Start date
- October 1, 2026
- Primary completion date
- December 1, 2026
- First posted
- January 13, 2025
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT06771024
- Registry last updated
- September 10, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT06771024 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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