NCT07578090

Brief Summary

This project aims to develop a community-based health promotion intervention model for populations at potential risk of metabolic syndrome. Through exercise training and lifestyle modifications, the project seeks to improve cardiopulmonary function and disease control, align with current public health policies, and establish an evidence-based model with strong potential for broader implementation.

Trial Health

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Trial Health Score

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

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
7mo left

Started May 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

April 27, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

May 11, 2026

Completed
20 days until next milestone

Study Start

First participant enrolled

May 31, 2026

Expected
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

May 11, 2026

Status Verified

March 1, 2026

Enrollment Period

7 months

First QC Date

April 27, 2026

Last Update Submit

May 4, 2026

Conditions

Keywords

hypertensionexercise trainingcardiovascular diseasehyperlipidemiahyperglycemia

Outcome Measures

Primary Outcomes (2)

  • appendicular skeletal muscle mass index

    appendicular skeletal muscle mass (ASM) divided by height squared; low muscle mass is defined as ASMI \< 7.0 kg/m² in men and \< 5.7 kg/m² in women

    From enrollment to the end of intervention at 12 months

  • six minute walk test

    functional performance; higher scores mean a better outcome

    From enrollment to the end of intervention at 12 months

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patient of Affiliated University Hospital

You may qualify if:

  • Participants with hypertension, hyperglycemia, or hyperlipidemia who meet at least one of these criteria are eligible for enrollment.

You may not qualify if:

  • Age under 18 years
  • Patients diagnosed with neuromuscular disorders
  • Inability to perform cardiopulmonary exercise testing
  • Refusal to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fu Jen Catholic University Hospital, Fu Jen Catholic University

New Taipei City, 24352, Taiwan

Location

MeSH Terms

Conditions

HypertensionCardiovascular DiseasesHyperlipidemiasHyperglycemia

Condition Hierarchy (Ancestors)

Vascular DiseasesDyslipidemiasLipid Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesGlucose Metabolism Disorders

Study Officials

  • Ke-Yun Chao, PhD

    Fu Jen Catholic University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

April 27, 2026

First Posted

May 11, 2026

Study Start (Estimated)

May 31, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

May 11, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations