Emotion Regulation Intervention to Sustain Physical Activity in Rural-dwelling Women and Men After Myocardial Infarction

Completed · Not applicable

Conditions studied: Cardiac Event, Emotions

In brief

The purpose of this study is to evaluate early preliminary efficacy of the eMotion intervention in US adults who have experienced a first cardiac event and participating in phase II cardiac rehabilitation. This study will evaluate early efficacy and evaluate the cognitive processes as intervention response variables. Investigators will also examine the relationships between emotion regulation and other cognitive processes and symptoms (threat and stress, cognition and motivation), symptoms \[depression, anxiety, pain, sleep, and fatigue\]), and health related quality of life among adults enrolled in cardiac rehabilitation after a first cardiac event.

Key facts

Study ID: NCT04441086
Run by: Indiana University
People needed: 40
Starts: 2021-01-12
Expected to finish: 2023-10-10
Last updated by the study team: 2023-10-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

First time major cardiac event as documented in medical record;
enrolled in cardiac rehabilitation phase II program;
living independently; and
at least mild symptoms of depression and/or anxiety (determined by standardized measure cutpoints).

You may not qualify if…

does not speak English;
major Axis 1 psychiatric diagnosis (e.g. schizophrenia);
terminal cancer; and
legally blind

Where it is running

Indiana University Health West Hospital — Avon, Indiana, United States
Indiana University Health Bedford Hospital — Bedford, Indiana, United States
Indiana University Health Methodist Hospital — Indianapolis, Indiana, United States
Indiana University Health Tipton Hospital — Tipton, Indiana, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.