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IMST for Dementia Risk Reduction

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Secondary endpoints: details revised at 7 of 7 entries
    • Eligibility criteria shortened, about 3 words
  2. Minor Secondary endpoints: details revised at 2 of 7 entriesv3
  3. Minor Interventions: Inspiratory Muscle Strength Training (Device) to Inspiratory Muscle Strength Training High-Resistance (Device), Inspiratory Muscle Strength Training Low-Resistance (Device)
    • Secondary endpoints: 4 to 7
    • Study description revised
    v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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Using a 2-arm, RCT approach, the primary goal of the study is to evaluate the feasibility and preliminary efficacy of Inspiratory Muscle Strength Training (IMST) as a non-pharmacologic intervention to reduce cardiovascular and cognitive risks in older adults. Next, investigators will examine secondary effects of IMST on mood, sleep quality, systemic inflammation, and physical/motor function. Finally, investigators will assess participant adherence and acceptability ratings of using an 8-week home-based IMST protocol in a diverse older adult sample.
Trial Details
NCT Number NCT07349706
Lead Sponsor Florida State University
Collaborators: National Institutes of Health (NIH)
Conditions
(from sponsor)
Systolic Blood Pressure, Blood Pressure, Depression - Major Depressive Disorder, Anxiety, Sleep Quality, Physical Function, Cognitive Function
Related terms Anxiety Disorders, Sleep Initiation and Maintenance Disorders
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov