Improving Frailty in Patients With Stable Ischemic Heart Disease
FRAGICOR
Impact of a Program Aimed at Improving Frailty in Patients With Stable Ischemic Heart Disease in Primary Care: Fragicor Study
2 other identifiers
interventional
60
1 country
1
Brief Summary
The goal of this clinical trial is to improve the frailty in old patients who have a cardiac disease . Researchers will determine the improvement in the instability and the strength along twelve sessions based on guided exercises and mobility techniques made by physiotherapists. Research team will also evaluate the medications and diet, as well as laboratory and clinical tests.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 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
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2025
CompletedFirst Submitted
Initial submission to the registry
December 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedFirst Posted
Study publicly available on registry
January 28, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
ExpectedJanuary 28, 2026
January 1, 2026
3 months
December 2, 2025
January 22, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Short Physical Performance Battery (SPPB) components (balance, gait speed, chair rise)
Improvement in baseline values: each of the three component scores \<= 4 points, and tests consists of: balance test, Gait speed and chair-stand tests. Maximum possible is 12 points and under 10 points means frailty
From enrollment to the end of treatment ending after 12 weeks.
Secondary Outcomes (1)
Euroqol5D Goldberg Anxiety and Depression Scale Number of falls throughout the study Major Cardiovascular events Adherence to the program
from the baseline to 12 weeks of intervention
Study Arms (1)
Patients with stable coronary heart disease
EXPERIMENTALolder than 70 years, idependents in ADL
Interventions
Primary care based physiotherapy groups
Eligibility Criteria
You may qualify if:
- Age ≥ 70 years
- Diagnosis of coronary artery disease (International Classification Diseases (ICD)-10 I20-I25)
- Canadian Cardiovascular Society Class I
You may not qualify if:
- Inability or refusal to provide informed consent (advanced dementia, severe psychiatric illness)
- Inability to perform protocol procedures
- Severe mobility-limiting conditions (Parkinson's disease, progressive neurological disorders, disabling joint disease)
- Recent (\<6 months) unstable angina, myocardial infarction, coronary revascularization or angioplasty
- Deep venous thrombosis or pulmonary embolism in the last 6 months
- Recent stroke (\<6 months)
- Heart failure in New York Heart Assocaition functional status (NYHA) III-IV
- Left ventricular ejection fraction \< 50%
- Symptomatic valvular heart disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Primary Care Centers
Barcelona, Select..., 08007, Spain
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 2, 2025
First Posted
January 28, 2026
Study Start
October 1, 2025
Primary Completion
December 30, 2025
Study Completion (Estimated)
December 31, 2026
Last Updated
January 28, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share