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Multicomponent Exercise and Postural Hygiene

NCT07632495 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-06-08

No results posted yet for this study

Summary

This non-randomized clinical study aims to evaluate whether a multicomponent physical exercise program with integrated postural hygiene can improve functional capacity, postural risk, musculoskeletal symptoms, health-related quality of life, and body composition in adult and older women. Eighty participants are allocated to three groups: an experimental group performing exercise with integrated postural hygiene, a reference group with previous postural hygiene training performing the same intervention, and a control group performing the same exercise program without the postural hygiene component. Participants are assessed before, during, and after the intervention, as well as at follow-up. The broader research project also includes a separate cross-sectional observational component designed to describe postural habits, musculoskeletal symptoms, and functional health-related variables in women enrolled in a community-based Maintenance Gymnastics program.

Conditions

  • Postural Hygiene

Interventions

BEHAVIORAL

Multicomponent physical exercise with integrated postural hygiene

Structured multicomponent physical exercise program including strength, balance, mobility, and postural control exercises, with integrated postural hygiene strategies during exercise execution and activities of daily living. Sessions will be conducted in the usual practice context, following a previously established common protocol and with implementation control by program instructors. This intervention will be assigned to the two arms with integrated postural hygiene.

BEHAVIORAL

Multicomponent physical exercise without postural control

Structured multicomponent physical exercise program including strength, balance, and mobility exercises, delivered without the specific postural control component. Sessions will be conducted in the usual practice context, following a previously established common protocol and with implementation control by program instructors. This intervention will be assigned to the active comparator arm without postural control.

Sponsors & Collaborators

  • Catholic University of Murcia

    lead OTHER

Principal Investigators

  • Ana I. Rodrigo · Catholic University of Murcia

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
82 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-06-30
Primary Completion
2026-09-30
Completion
2026-09-30

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07632495 on ClinicalTrials.gov