Breast Cancer Clinical Trial

Fatigue in Breast Cancer Patients Undergoing Radiotherapy-eSMART-MH

Summary

The purpose of this study is to determine if an avatar-based depression self-management intervention (eSMART-MH) once a week for the duration of the participant's radiation treatment will significantly reduce depressive symptoms. Investigators also seek to explore how women with breast cancer describe their mood using prompted and unprompted speech through electronic social media and interviews.

Participants will be randomized into the eSMART-MH group or the theater testing (attention control) group. In addition to the assigned interventions, participants will be asked to complete questionnaires and interviews with the study staff.

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Full Description

The purpose of this study is to determine if an avatar-based depression self-management intervention (eSMART-MH) once a week for the duration of the participant's radiation treatment will significantly reduce depressive symptoms. Investigators also seek to explore how women with breast cancer describe their mood using prompted and unprompted speech through electronic social media and interviews.

Participants will be randomized into the eSMART-MH group or the theater testing (attention control) group. In addition to the assigned interventions, participants will be asked to complete questionnaires and interviews with the study staff.

Participants will be enrolled within two weeks of radiotherapy. A preliminary depression survey (IDS-SR) will be given to assess depression. There will be a total of three routine study assessments, one within two weeks prior to the beginning of radiotherapy, one the last week of radiotherapy and one 5 - 7 weeks after radiotherapy is completed.

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Eligibility Criteria

Inclusion Criteria:

Patients seen in the Emory Breast Center at The Emory Clinic and Emory Midtown Hospital who are treated with curative intent.
Score of 8 or higher on the Inventory of Depressive Symptomology - Self Reported (IDS-SR) test

Study is for people with:

Breast Cancer

Study ID:

NCT02759549

Recruitment Status:

Withdrawn

Sponsor:

Emory University

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There is 1 Location for this study

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Emory Clinic
Atlanta Georgia, 30322, United States
Emory University Hospital Midtown
Atlanta Georgia, 30322, United States
Emory University Hospital
Atlanta Georgia, 30322, United States
Winship Cancer Institute
Atlanta Georgia, 30322, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Study ID:

NCT02759549

Recruitment Status:

Withdrawn

Sponsor:


Emory University

How clear is this clinincal trial information?

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