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Heart failure patients get a virtual coach: study tests remote motivational interviews

NCT ID NCT07413419

Disease control Sponsor: Wroclaw Medical University Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether remote motivational interviewing—online chats with a trained nurse—can help heart failure patients and their family caregivers improve self-care and quality of life. 600 participants (300 patients with moderate to severe heart failure and their caregivers) will receive the coaching over 12 months. The goal is to see if this approach helps with medication, diet, and symptom monitoring, reducing hospital visits and easing caregiver burden.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 600 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Jan 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adult patients aged 18 years or older. * Diagnosis of heart failure. * New York Heart Association (NYHA) functional class II-IV. * Poor self-care as assessed at baseline. * Receiving care at the participating heart failure clinic. * Access to the internet and a device capable of videoconferencing. * Ability to understand the study procedures and provide written informed consent. * Having an identified primary informal caregiver willing to participate in the study. * Informal caregivers aged 18 years or older. * Caregivers identified by the patient as the primary person providing unpaid support in daily disease management. * Caregivers able to understand the study procedures and provide written informed consent. Exclusion Criteria: * Severe cognitive impairment that would limit the ability to participate in the intervention or complete study assessments. * Acute coronary syndrome or other acute cardiac event within the last 3 months. * Residence in a nursing home or long-term care facility. * Inability to participate in videoconferencing sessions. * Participation in another interventional study that could interfere with the outcomes of this trial.

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Conditions

The condition(s) this trial relates to.

heart failure

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Caregiver Heart failure (HF) Motivational interviewing (MI) Self-care

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • University Clinical Hospital in Wroclaw

    Wroclaw, 51-618, Poland

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