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Coronary Heart DiseaseFRAGICORNCT07373119

Improving Frailty in Patients With Stable Ischemic Heart Disease

A study testing physiotherapy in people with Coronary Heart Disease, run by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina at 1 site in Spain.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 70 years and older
Conditions the study is for
Coronary Heart Disease
What is being tested?
physiotherapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteSpain
Study dates
1 Oct 2025to 31 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 70 years and older
  • All sexes
  • No healthy volunteers
  • Older adult

Who may be able to join

  • Age ≥ 70 years
  • Diagnosis of coronary artery disease (International Classification Diseases (ICD)-10 I20-I25)
  • Canadian Cardiovascular Society Class I
  • Low cardiovascular risk according to exclusion criteria

Who cannot join

  • 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)
Show all 9Show fewer
  • Heart failure in New York Heart Assocaition functional status (NYHA) III-IV
  • Left ventricular ejection fraction < 50%
  • Symptomatic valvular heart disease

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Spain1 site
  • Primary Care Centers

    Barcelona, Select..., 08007

Other trials in Spain

About this study

Official title: Impact of a Program Aimed at Improving Frailty in Patients With Stable Ischemic Heart Disease in Primary Care: Fragicor Study

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.

Read the detailed description

Intitial visit to measure quality of life, instability and strenght, followed by twelve sessions, one each week will be performed

Being tested
physiotherapy
Keywords
frailty, coronary heart disease, elderly
Medical subject headings
Coronary Disease, Frailty

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07373119
Study groupRoleWhat they receive
Patients with stable coronary heart diseaseExperimentalolder than 70 years, idependents in ADL
Receives: Other: physiotherapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

    Measured: From enrollment to the end of treatment ending after 12 weeks.

Secondary outcomes (1)
  1. Euroqol5D Goldberg Anxiety and Depression Scale Number of falls throughout the study Major Cardiovascular events Adherence to the program

    Euroqol5D measures the Quality of life through an Analogic Visual Scale, which ranks from 0 (worst) to100(best) Goldberg anxiety and depression scales measure the probabilty of suffering from anxiety or depression. The tests consist in a total of 9 questions for each dimension. A score of >=4 in any of the dimensions suggest pathology.

    Adherence to the program will be evbaluated counting the attendance to the sessions. More than 9 sessions will be considerated good adherence

    Measured: from the baseline to 12 weeks of intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Jan 2026
  2. Study start1 Oct 2025
  3. Primary completion30 Dec 2025
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Model description
It is an experimental study before-after based on a program of 12 sessions of physiotherapy in primary care setting
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07373119
Sponsor's protocol ID
ethics committee 25/198-P
Other IDs
Ajuts XB
Acronym
FRAGICOR
Status last verified
Jan 2026
First submitted
2 Dec 2025
Last updated
28 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing physiotherapy in people with Coronary Heart Disease, run by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 28 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Short Physical Performance Battery (SPPB) components (balance, gait speed, chair rise) (time frame: From enrollment to the end of treatment ending after 12 weeks.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jan 2026.

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