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Feasibility of a Community-Integrated Isometric Handgrip Exercise Program and Its Preliminary Effects on Blood Pressure and Cognitive Function in Older Adults

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 7 months later Sep 15, 2026 → Apr 15, 2027
See other at-risk trials from McMaster University

Record History

  1. Primary and study completion pushed from Sep 15, 2026 to Apr 15, 2027 Recruitment opened · Start date changed from estimate of Jul 28, 2026 to Aug 18, 2026 · Eligibility criteria expanded, about 13 words · 2 more Show 5 more changesShow less
    • Recruitment opened
    • Start date changed from estimate of Jul 28, 2026 to Aug 18, 2026
    • Eligibility criteria expanded, about 13 words
    • Secondary endpoints: details revised at 17 of 17 entries
    • Site details revised at 2 of 2 sites
  2. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
McMaster University
191 trials monitored
See 14 trials at risk
Hypertension
1,795 trials monitored
See 85 trials at risk
The goal of this clinical trial is to evaluate whether a short, supervised isometric handgrip exercise program is feasible and acceptable for older adults with elevated blood pressure or hypertension. It will also explore whether this type of exercise may improve blood pressure and cognitive function. The main questions it aims to answer are: * Is this handgrip exercise program practical and acceptable for older adults to participate in within a community exercise setting? * Does participation in the program lead to changes in blood pressure and cognitive function? Researchers will compare two handgrip devices to determine whether the method of delivering the exercise influences feasibility and outcomes. Participants will: * Be randomly assigned to use one of two handgrip devices. * Complete supervised exercise sessions twice per week for 4 weeks. * Perform brief handgrip contractions at a set intensity during each session. * Complete blood pressure and cognitive assessments before and after the program.
Trial Details
NCT Number NCT07648498
Lead Sponsor McMaster University
Conditions Hypertension, Elevated Blood Pressure
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov