No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
45 (estimated)
Sponsor
Medical University of South Carolina · Other
Who this trial is looking for
This trial is looking for cancer survivors who have symptoms of depression. Participants will either use a mobile app for depression treatment or have telehealth sessions for 10 weeks, while answering questionnaires about their experience in the study.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old
I am a cancer survivor
I have symptoms of depression
I am not currently receiving any depression treatment
I can use a telehealth service and the Moodivate app
I have a valid email address or can receive texts for assessments
I speak English
You may not be able to join if
I have had suicidal thoughts recently
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 p…
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.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria:
* age 18+
* cancer survivor
* current elevated depressive symptoms defined per ASCO as a PHQ-9 score ≥ 8
* not currently receiving psychosocial depression treatment
* have the ability to complete treatment via telehealth and use Moodivate
* have a valid e-mail address or text me…
Inclusion Criteria:
* age 18+
* cancer survivor
* current elevated depressive symptoms defined per ASCO as a PHQ-9 score ≥ 8
* not currently receiving psychosocial depression treatment
* have the ability to complete treatment via telehealth and use Moodivate
* have a valid e-mail address or text message access (for assessments)
* English fluency
Exclusion Criteria:
\- Current suicidal ideation at final eligibility screening (PHQ-9 item 9 ≥1)
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