NCT06842849

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
140

participants targeted

Target at P50-P75 for not_applicable

Timeline
8mo left

Started Oct 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress45%
Oct 2025Dec 2026

First Submitted

Initial submission to the registry

February 18, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 24, 2025

Completed
8 months until next milestone

Study Start

First participant enrolled

October 22, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 30, 2026

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

9 months

First QC Date

February 18, 2025

Last Update Submit

April 27, 2026

Conditions

Keywords

old adultsexerciseaccelerometry

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

EXPERIMENTAL

Carrying out an exercise program one year in progress

Other: Exercise program

Exercise T1

EXPERIMENTAL

Carrying out an exercise program without prior exercise

Other: Exercise program

Control

NO INTERVENTION

Control

Interventions

Multimodal and multicompetent exercise program 2 days a week for 60 minutes and 1 day of walking exercise for 60 minutes.

Exercise T0Exercise T1

Eligibility Criteria

Age59 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

FrailtyMotor Activity

Interventions

Resistance Training

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsBehavior

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • CARMEN GARCÍA GOMARIZ

    UNIVERSITAT DE VALÉNCIA DEPARTAMENTO D'INFERMERIA

    PRINCIPAL INVESTIGATOR

Central Study Contacts

CARMEN GARCÍA GOMARIZ, Phd

CONTACT

CARMEN GARCÍA GOMARIZ

CONTACT

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

Locations