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Sleep Extension to Improve Sleep Efficiency and QoL in HF With Preserved Ejection Fraction: the SLEEP-HF Pilot Study

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Enrolling

Conditions

Heart Failure With Preserved Ejection Fraction

Treatments

Behavioral: Sleep Hygiene Training
Behavioral: Customized Sleep Coaching

Study type

Interventional

Funder types

Other

Identifiers

NCT06567925
HM20028346

Details and patient eligibility

About

Nearly one-third of US adults have poor sleep quality. Sleep quality refers to sleep efficiency, sleep latency, sleep duration, wake after sleep onset, and movement during the night. Specifically, sleep efficiency (SE) measures how well an individual utilizes their time in bed for restorative sleep and it highly depends on actual sleep duration. Reduced SE is associated with a greater risk for heart failure (HF), which affects ~6.7 million adults in the US alone. HF with preserved ejection fraction (HFpEF) accounts for about half of all HF diagnoses and is associated with poor prognosis (30-50% 5-year mortality from diagnosis) and severely reduced quality of life (QoL). Long-term goal for the investigators is to identify sleep modulation as a potential therapeutic target to improve QoL in HFpEF, with poor SE being present in ~60% of patients with HFpEF. The study is aimed to see if the sleep modulation is feasible and modulating sleep can improve the QoL and functional capacity along with the reduction of inflammation among subjects with HFpEF.

Full description

The investigators plan a 2-week single-arm open-label feasibility study in 17 subjects with HFpEF with a 1-week run-in phase (3 weeks total duration) with a sleep extension intervention combined with sleep hygiene training to improve SE in patients with symptomatic HFpEF. The investigator's primary endpoint is to increase sleep duration and efficiency with this intervention.

Enrollment

17 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • confirmed clinical diagnosis of stable HF (NYHA class II-III)
  • left ventricular ejection fraction>50% documented in the prior 12 months
  • aged ≥18 years
  • habitual reported sleep duration ≤7 hours
  • sleep efficiency <85% measured during the 1-week run-in phase

Exclusion criteria

  • concomitant conditions that can limit physical activity
  • severe debilitating diseases (ischemic heart disease. angina, arterial fibrillation, moderate to severe valvular disease)
  • taking sleep medicine or melatonin irregularly
  • pregnancy
  • stage V kidney disease (with dialysis)
  • shift worker
  • insomnia
  • hospitalization within the last 2 months
  • patients with sleep and circadian disorders
  • fluid overload
  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers)
  • Pregnant women
  • Prisoners

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

17 participants in 1 patient group

Gradual sleep extension strategy
Experimental group
Description:
Demonstrate the feasibility of a gradual sleep extension strategy combined with sleep hygiene training aimed at increasing sleep efficiency in patients with heart failure with preserved ejection fraction on guideline-directed medical therapy
Treatment:
Behavioral: Sleep Hygiene Training
Behavioral: Customized Sleep Coaching

Trial contacts and locations

1

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Central trial contact

Syed Imran Ahmed; Salvatore Carbone

Data sourced from clinicaltrials.gov

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