Mental Stress Reactivity in Women With CMD

NARecruitingINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

July 19, 2022

Primary Completion Date

September 30, 2026

Study Completion Date

December 31, 2026

Conditions
Post-menopause
Interventions
OTHER

Study Procedures

"All participants will answer a series of questionnaires that address several factors such as patient medical history, family history, medication usage, health behaviors, psychological factors, etc. Questionnaires related to symptoms, psychological factors, depression, anxiety, and quality of life will be taken.~All participants will undergo 123I-MIBG SPECT imaging in the morning in a fasting state. Mental Stress Testing will be conducted in the Laboratory in the morning after fasting for at least 4 hours and withdrawal of all vasoactive medications, caffeine, and tobacco 24-48 hours before testing. Participants will also undergo 1-week of Home Monitoring using a single-use, noninvasive, water-resistant, 7-day ambulatory ECG monitoring, which offers the advantage of direct access to raw data that can be downloaded from the device after use.~A 3-day food recall diary, cognitive assessments via the NIH Toolbox, and a Sleep diary during home monitoring will be collected."

Trial Locations (4)

30308

RECRUITING

Emory Hospital Midtown, Atlanta

RECRUITING

Emory Saint Joseph's Hospital, Atlanta

30322

RECRUITING

Emory Clinic, Atlanta

RECRUITING

Emory Hospital, Atlanta

All Listed Sponsors
collaborator

National Heart, Lung, and Blood Institute (NHLBI)

NIH

lead

Emory University

OTHER