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NCT07184541Recruiting

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

The Effect of a Nurse-led Daily Weight Monitoring Intervention (Wake and Weigh) on Heart Failure Quality of Life and Self-care

Source: ClinicalTrials.gov · Last updated 24 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Ongoing self-care for heart failure is essential to avoid complications and hospitalization. Supportive strategies are needed; however, patients with heart failure may find many interventions complicated and overwhelming. The purpose of this pilot study is to implement a simple weight tracking tool (Wake and Weigh) to affect self-care and quality of life in a population of older adults with heart failure. This will be a randomized controlled pilot trial to test the methods to be used in a larger randomized controlled trial. The Self-care in Heart Failure Index and Kansas City Cardiomyopathy Questionnaire surveys will be given at admission and four weeks after discharge. The Wake and Weigh tool is designed to help patients track weight in the hospital and following discharge. Feasibility endpoints will be summarized descriptively.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
42 (estimated)
First submitted
23 Feb 2025
Start date
Nov 2024
Primary completion date
Oct 2026
Lead sponsor
Lee Anne Siegmund
NCT number
NCT07184541

What you commit to

  • Study type: Interventional
  • Planned participants: 42
  • From Nov 2024 to the primary completion date, Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Documented diagnosis of cognitive impairment.

Other

  • A Charlson Comorbidity Index (CCI) of \>4. This was chosen to exclude patients more likely to have hospital stays longer than a week. A CCI of \>3 was based on research showing a relationship to mortality (Imam et al., 2020), a CCI of ≥ 6 with a 2.8-times higher mortality (Yilmaz \& Omurlu, 2019), and likelihood of longer hospital length of stay for patients with HF if CCI \>2 (Foraker et al., 2014).

Who the study is looking for

  • Adults (55 years or older)
  • New or existing diagnosis of HF (regardless of type or length of time since diagnosis).
  • Being treated for HF signs and/or symptoms during the current hospitalization (any of the following: IV diuretic, fluid restriction, low sodium diet).
  • Must be able to read and communicate in English.
  • Must be able to stand and weigh independently.
  • Must have a scale at home, or ability to obtain one for the study.

Age in the registry: 55 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cleveland Clinic Avon Hospital
Coordinator of this site? Confirm its status
AvonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.