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Physical Activity intervention arm for Physical Activity
N/A
Waitlist Available
Led By Charles B Eaton, MD, MS
Research Sponsored by Memorial Hospital of Rhode Island
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* alive, community dwelling
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 4 years of randomization
Awards & highlights
No Placebo-Only Group
Summary
The WHISH-2-Prevent Heart Failure (HF) study is an ancillary study to the Women's Health Initiative Strong and Healthy (WHISH) exercise pragmatic trial. The WHISH-2-Prevent HF trial examines the intervention effect of physical activity (PA) on both incident HF and HF burden (recurrent HF and CVD death in those with HF) in a cost effective manner in elderly women. In addition, it will allow a dose-finding analysis to better understand the type, intensity and frequency of PA that leads to a reduced risk and burden of HF. The focus of the parent WHISH trial is on atherosclerotic cardiovascular disease and not heart failure.
Eligible Conditions
- Physical Activity
- Female
- Heart Failure
- Strength Training
- Aging
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within 4 years of randomization
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within 4 years of randomization
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Heart failure
Secondary study objectives
Cardiovascular disease mortality
Heart failure with preserved ejection fraction
Heart failure with reduced ejection fraction
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Physical Activity intervention armExperimental Treatment1 Intervention
Receive a tailored behavioral interventions for exercise and strength training via multiple channels including frequent mailings, integrated voice response and outreach phone calls, interactive website, and referral to local community exercise resources.
Group II: Control armActive Control1 Intervention
Receive general health mailings
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Physical Activity
2019
Completed Phase 3
~4760
Find a Location
Who is running the clinical trial?
Wake Forest UniversityOTHER
191 Previous Clinical Trials
115,135 Total Patients Enrolled
University at BuffaloOTHER
132 Previous Clinical Trials
49,000 Total Patients Enrolled
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,922 Previous Clinical Trials
47,710,802 Total Patients Enrolled
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