Impact of a Physical Exercise Program in a Rural Area
1 other identifier
interventional
140
1 country
1
Brief Summary
With this work we want to assess whether there are differences in the amount of physical activity per week, measured by accelerometry in 3 groups of subjects, where one group (G1) has been carrying out a PA program called "Enguera Sé Saludable" for a year. another group (G2) newly introduced to the same exercise program, and a control group (G3) that does not carry out an exercise program but declared itself active.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 18, 2025
CompletedFirst Posted
Study publicly available on registry
February 24, 2025
CompletedStudy Start
First participant enrolled
October 22, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
April 28, 2026
April 1, 2026
9 months
February 18, 2025
April 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
MVPA
Mooderate to vigorous amount of activity. Assess the amount of moderate to vigorous exercise during accelerometry for one week.
1 year
Secondary Outcomes (9)
Up & Go
1 year
Tinetti
1 year
SPBB
1 YEAR
Sit to Stand Test
1 year
IPAQ
1 year
- +4 more secondary outcomes
Study Arms (3)
Exercise T0
EXPERIMENTALCarrying out an exercise program one year in progress
Exercise T1
EXPERIMENTALCarrying out an exercise program without prior exercise
Control
NO INTERVENTIONControl
Interventions
Multimodal and multicompetent exercise program 2 days a week for 60 minutes and 1 day of walking exercise for 60 minutes.
Eligibility Criteria
You may qualify if:
- Adults over 59 years of age.
- Patients who comply with accelerometer times for 7 days.
- Patients who correctly complete the accelerometer registration sheet.
- Patients who complete the informed consent
You may not qualify if:
- Patients who do not wear the accelerometer 600 minutes a day for at least 3 days on weekdays and 480 minutes for at least 1 day on the weekend.
- 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).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Universitat de València
Valencia, 46010, Spain
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
CARMEN GARCÍA GOMARIZ
UNIVERSITAT DE VALÉNCIA DEPARTAMENTO D'INFERMERIA
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor of Nursing
Study Record Dates
First Submitted
February 18, 2025
First Posted
February 24, 2025
Study Start
October 22, 2025
Primary Completion (Estimated)
July 30, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
April 28, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share