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Effects of Physical Exercise on Frailty, Mental and Physical Health of Older Adults in Rural Areas. (Rural-Frail)

U

University of Zaragoza

Status

Enrolling

Conditions

Old Age
Frailty

Treatments

Device: Face-to-face and video-assisted training

Study type

Interventional

Funder types

Other

Identifiers

NCT06556537
PID2022-140622OA-I00.

Details and patient eligibility

About

Global aging is a significant challenge, both economically and in terms of public health. One of the main challenges is to maintain the health and functionality of older adults. Physical exercise has been suggested as one of the best non-pharmacological tools to prevent health and functionality loss. However, existing scientific literature has mainly focused on older adults from urban centers. There are no studies focused on older people in rural areas, who have particular characteristics.

The present project aims to evaluate the effects of a face-to-face and video-assisted intervention, which incorporates multi-component physical exercise with different motivational strategies, on the mental health, physical function, and frailty of individuals over 65 years of age residing in rural areas. Additionally, it aims to determine the effectiveness, safety, and adherence of new technologies in carrying out an intervention that includes multi-component physical exercise, cognitive work, and motivational strategies through video assistance for older women and men living in rural areas.

A randomized controlled trial will be conducted, involving 240 people over the age of 65 who will be randomly divided into two groups. One group, the intervention group, will participate in a face-to-face multicomponent physical exercise program three times a week for 60 minutes per session over 12 weeks. After that, the intervention will continue through video-assisted sessions for the remaining nine months, divided into three blocks of two months of rest and one video-assisted intervention. The control group will continue with their usual daily activities but receive recommendations for physical activity and mental and physical health talks. Both groups will undergo a battery of tests to evaluate the effects of the interventions. The primary variable measured will be functional capacity, assessed through the Short Physical Performance Battery. Secondary variables will include health-related physical condition (Power frail app), cognitive function (Trail making test), and quality of life, among others.

The results expected from this study will be of significant scientific and technical importance in the field of psycho-socio-health. Consequently, the project is of utmost importance, not only to enhance the health of the rural population but also to promote individual and social sustainability.

Enrollment

240 estimated patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age equal to or greater than 65 years.
  • Be able to provide informed consent voluntarily.
  • Walk autonomously.
  • Have a score of 4 points or more on the Short Physical Performance Battery (SPPB).

Exclusion criteria

Those that have to do with contraindications for performing physical exercise:

  • Recent acute myocardial infarction within the last 3-6 months or unstable angina.
  • Uncontrolled atrial or ventricular arrhythmias.
  • Dissecting aortic aneurysm.
  • Severe aortic stenosis.
  • Acute endocarditis or pericarditis.
  • Uncontrolled arterial hypertension (>180/100 mmHg).
  • Acute thromboembolic disease.
  • Acute and severe heart or respiratory failure.
  • Recent bone fracture, orthostatic hypotension.
  • Diabetes or uncontrolled hypoglycemia.
  • Any pathology that causes a significant functional limitation such as advanced Parkinson's, considerable vision or hearing problems Cancer, or autoimmune disease.
  • People scoring less than 4 on the SPPB (dependents).
  • Any pathology or circumstance that the primary care team considers counterproductive to participation in physical exercise.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

240 participants in 2 patient groups

Intervention group
Experimental group
Description:
Participants will undergo a face-to-face and video-assisted physical exercise intervention.
Treatment:
Device: Face-to-face and video-assisted training
Control group
No Intervention group
Description:
Participants in the control group will maintain their usual lifestyle throughout the project. They will receive physical activity recommendations for older people and will attend monthly health promotion meetings.

Trial contacts and locations

1

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Central trial contact

Ángel Matute-Llorente, PhD

Data sourced from clinicaltrials.gov

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