This trial is terminated!
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More info
You can access this
clinical trial
if you have
Ischemic Heart Disease
and you are
over 21
years old
-
The phase for this study is not defined.
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The purpose

This is a single center, randomized controlled trial which will include women with ischemic heart disease to receive either a self-directed stress reduction program delivered through a smart-phone application or activity tracking only for the first month ("early SR intervention" and "delayed SR intervention", respectively). Patients will be monitored for 1 month for application use and step counts via telephone or email interview and/or collection of screen-captured data. Baseline questionnaires will be repeated at the end of one month to assess for all primary and secondary measures, at which time the control group (activity tracking only) will be introduced to the intervention program. The early SR intervention group will not receive a new intervention but will be encouraged to continue using the app. Data will be collected for an additional 2 months with all participants in both groups. After the three-month study period, the study will close with the collection of final questionnaire data.

Provided treatments

  • Behavioral: Early SR intervention
  • Behavioral: Delayed SR intervention

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02893579. The sponsor of the trial is NYU Langone Health and it is looking for 6 volunteers for the current phase.
Official trial title:
Smartphone-delivered Stress Reduction Intervention for Women With Ischemic Heart Disease