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Clinical Trials in Portugal / NCT06722976
Enrolling by invitation Not applicable

Digital Health and Exercise for Autonomous Longevity Program

NCT06722976 · tracked via the Priya Life Science Portugal tracker
Phase
Not applicable
Started
2024-11-05
Last updated
2024-12-12

Condition(s) studied

Mild Cognitive Impairment (MCI)Older People

Investigational drug(s) / intervention(s)

Multicomponent exercise programs

Multicomponent exercise programs: The program is organized into three phases: (1) Initial assessment; (2) Multicomponent training sessions; (3) Final assessment. 1. The initial assessment will consist of physical fitness tests (lasting around 1 hour) and Neuropsychological Assessment tests (lasting around 1.5 hours). 2. The multicomponent training sessions will last 3 months, twice a week, 50 minutes each session. 3. The final assessment will be the same as the initial assessment (physical fitness tests (about 1 hour) and Neuropsychological Assessment tests (about 1.5 hours).

Study summary

Digital HEAL (Health and Exercise for Autonomous Longevity) is a multicomponent training program (combining concurrent training with cognitive stimulation) designed to promote physical fitness and cognitive function in older adults. This program merges a community-based approach with a scientific research project aimed at comparing the effects of in-person and online concurrent training on cognitive function and functional capacity in this population.

The program is structured into three phases: (1) Initial Assessment; (2) Multicomponent Training Sessions; (3) Final Assessment.

1. Initial Assessment The initial assessment will consist of physical fitness tests (approximately 1 hour) and Neuropsychological Evaluation tests (approximately 1.5 hours).
2. Multicomponent Training Sessions The multicomponent training sessions will last for 3 months, with a frequency of two sessions per week, each lasting 50 minutes, conducted in person at the institution.
3. Final Assessment The final assessment will be identical to the initial assessment, comprising physical fitness tests (approximately 1 hour) and Neuropsychological Evaluation tests (approximately 1.5 hours).

Expected Benefits The anticipated benefits for participants include significant improvements in physical fitness, with a particular emphasis on strength, balance, and motor autonomy, which play an essential role in fall prevention. Additionally, cognitive abilities such as orientation, memory, and brain plasticity are expected to improve. The program also aims to promote social interaction, reducing social isolation among older adults. Furthermore, the program will support participants\' maintenance within the institution, which helps preserve their routine and address mobility and accessibility limitations. This intervention will also help reduce costs and time for the institution.

Potential Risks The risks associated with participation in the program are similar to those inherent in any physical activity. However, the equipment and environment (floor type, lighting, temperature) are evaluated to ensure suitability for safe exercise at any age. The exercises are supervised by a qualified professional who takes special care to minimize exercise-related risks.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Male and female participants aged ≥ 65 years. * A score of ≥ 3 on the Short Physical Performance Battery (SPPB). * Willingness to participate in the training programs and collaborate with the research team. Ability to provide informed consent, either oral or written. Exclusion Criteria: * A score of ≤ 3 on the Short Physical Performance Battery (SPPB). * Presence of severe comorbidities that would negatively impact participation in the training program. * Presence of color blindness. * Diagnosis of severe dementia or severe impairment across multiple dimensions of cognition, which would prevent participation in the training program. * History of surgeries or fractures within the last 6 months. These criteria ensure that participants are suitable for the program and capable of engaging in the training sessions effectively.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Departement of Sports Science Covilha Covilhã

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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 NCT06722976 on ClinicalTrials.gov ↗ ← All trials in Portugal