Nurse-Led Weight Monitoring for Heart Failure

This study is testing a simple tool called "Wake and Weigh" to help people with heart failure (HF) better manage their condition and improve their quality of life. The Wake and Weigh tool provides instructions for daily weight monitoring. We want to see if this nurse-led intervention is easy for patients to use and if it can be studied on a larger scale. Participants will be adults aged 55 or older who have heart failure and are currently in the hospital for their symptoms. Half of the participants will use the Wake and Weigh tool, and the other half will receive standard heart failure information. We are looking to enroll 42 people. The study's current status is unclear.

Study design
This is a randomized controlled pilot study with 42 participants. It aims to test methods for a larger study in the future.
What's involved
Participants will use the Wake and Weigh tool or receive a heart failure handbook. Surveys will be given at admission and four weeks after discharge.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed from enrollment to the end of treatment at 4 weeks post-discharge.

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NCT07184541

A Nurse-Led Weight Monitoring Intervention For Heart Failure Quality of LIfe and Self-Care

Recruiting
NAAges 55+InterventionalSupportive care
Lee Anne Siegmund
~42 participants
Updated 2025-09-24 on ClinicalTrials.gov
What's tested:Wake and WeighUsual care

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Project Feasibility-fidelity
Measured over From enrollment to the end of treatment at 4 weeks post-discharge
+5 more outcomes measured
Heart Failure

NCT07184541

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Cleveland Clinic Avon Hospital

    Avon, Ohiostudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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  • Project Feasibility-fidelityFrom enrollment to the end of treatment at 4 weeks post-discharge

    Determine intervention fidelity by examining unintended variations in intervention implementation by nurse investigators

  • Project feasibility-use of toolFrom enrollment to the end of treatment at 4 weeks post-discharge

    Evaluate use (versus no use) of the Wake and Weigh tool by participants.

  • Project feasibility-recruitmentFrom enrollment to the end of treatment at 4 weeks post-discharge

    Assess how long it takes to recruit 10% of the anticipated larger sample size

  • Project feasibility-randomizationFrom enrollment to the end of treatment at 4 weeks post-discharge

    Assess retention in each randomized group

  • Project feasibility-appropriateness of SCHFIFrom enrollment to the end of treatment at 4 weeks post-discharge

    Determine percentage of completed SCHFIs

  • Project feasibility-appropriateness of KCCQFrom enrollment to the end of treatment at 4 weeks post-discharge

    Determine percentage of completed KCCQs