Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06930729

Optimizing Care for Cancer Survivors With Depression: Project 3

Led by Medical University of South Carolina · Updated on 2025-08-21

45

Participants Needed

1

Research Sites

39 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this research study is to evaluate different depression treatment approaches among cancer survivors. A cancer survivor is defined as anyone who is living and has been diagnosed with cancer. Participants will be randomly assigned to either receive a mobile app for depression treatment, called "Moodivate", or to receive telehealth depression treatment sessions. Approximately 2/3 of participants enrolled will receive the mobile app and the remaining 1/3 will receive depression treatment via telehealth. Participants that receive Moodivate may later be assigned to also receive depression treatment via telehealth based their response to the Moodivate app. Participants will be asked to either use the Moodivate app and/or receive depression treatment via telehealth for a period of 10 weeks. All participants will be asked to electronic questionnaire measures throughout the study period. Questionnaires will assess symptoms of depression, as well as general experiences using Moodivate and participating in this trial. Participation in this study will take about 24 weeks. Participation in this study may help improve options for emotional wellness for cancer survivors. The greatest risks of this study include frustration, worsening of emotional distress, data breach, and/or loss of confidentiality.

CONDITIONS

Official Title

Optimizing Care for Cancer Survivors With Depression: Project 3

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Cancer survivor
  • Current elevated depressive symptoms defined as PHQ-9 score of 8 or higher
  • Not currently receiving psychosocial depression treatment
  • Ability to complete treatment via telehealth and use the Moodivate app
  • Have a valid email address or text message access for assessments
  • Fluent in English
Not Eligible

You will not qualify if you...

  • Current suicidal thoughts at final eligibility screening (PHQ-9 item 9 score of 1 or higher)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Medical University of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

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Research Team

O

Olivia Levins

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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