Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
140 participants
INTERVENTIONAL
2025-10-22
2026-12-31
Brief Summary
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Detailed Description
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Analytical quasi-experimental study, with 3 groups. A group (G1) over 59 years of age, of both sexes who have been doing PA since the year before the start of the study, within the "Enguera Be Healthy" Program in the municipality of Enguera. Another group (G2) of both sexes, newly enrolled in the same exercise program over 59 years of age. A control group (G3) of 59 years of both sexes who do not carry out the exercise program, inhabitants of Enguera and apparently active. The data analyzed was obtained from the placement of an Actigraph model GT3X BT accelerometer for a week and the collection of data from the various instruments such as the measurement of blood pressure and weight using the Tanita BC Scale. -545N, the Tinetti scale, the Time Up \& Go test, the Monopodal Test, the SPPB test, the Sit to Stand Test, the Borg scale, the IPAQ questionnaire and the FHSQ questionnaire.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Exercise T0
Carrying out an exercise program one year in progress
Exercise program
Multimodal and multicompetent exercise program 2 days a week for 60 minutes and 1 day of walking exercise for 60 minutes.
Exercise T1
Carrying out an exercise program without prior exercise
Exercise program
Multimodal and multicompetent exercise program 2 days a week for 60 minutes and 1 day of walking exercise for 60 minutes.
Control
Control
No interventions assigned to this group
Interventions
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Exercise program
Multimodal and multicompetent exercise program 2 days a week for 60 minutes and 1 day of walking exercise for 60 minutes.
Eligibility Criteria
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Inclusion Criteria
* Patients who comply with accelerometer times for 7 days.
* Patients who correctly complete the accelerometer registration sheet.
* Patients who complete the informed consent
Exclusion Criteria
* Patients who suffer from illness during data collection.
* Patients who do not wear the accelerometer for 7 days. Be in IPAQ category 1 (low level of AF).
59 Years
ALL
Yes
Sponsors
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University of Valencia
OTHER
Responsible Party
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CARMEN GARCÍA GOMARIZ
Assistant Professor of Nursing
Principal Investigators
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CARMEN GARCÍA GOMARIZ
Role: PRINCIPAL_INVESTIGATOR
UNIVERSITAT DE VALÉNCIA DEPARTAMENTO D'INFERMERIA
Locations
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Universitat de València
Valencia, , Spain
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ESS_01
Identifier Type: -
Identifier Source: org_study_id
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