Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Mobile app for treating depression in cancer survivors

Official title: Evaluation of a Proactive Identification and Digital Mental Health Intervention Approach to Address Unmet Psychosocial Needs of Individuals Living With Likely Incurable Cancer

Run by Medical University of South Carolina · NCT06582784 · Data updated 2026-11-12

This study tests if a mobile app called 'Moodivate' can help cancer survivors who are feeling depressed feel better over 12 weeks.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment279 (estimated)
SponsorMedical University of South Carolina
Academic / other
Locations1 site (Charleston, South Carolina)
StatusRecruiting
StartedOctober 28, 2024
Main results expectedSeptember 1, 2028
Study endsSeptember 1, 2028
Registry record updatedMay 22, 2026
Trial IDNCT06582784 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults over 18 years old with likely incurable cancer and elevated depressive symptoms who own a smartphone and are willing to use a mobile app.

Probably not a fit

Patients with current suicidal ideation or severe cognitive impairment may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This research evaluates the effectiveness of a mobile application called 'Moodivate' designed to assist cancer survivors experiencing depression. Participants will be randomly assigned to either use the app or not, with approximately two-thirds receiving the app. Throughout the 12-week study, all participants will complete electronic questionnaires to assess their depressive symptoms and experiences with the app. The study aims to address the unique mental health needs of individuals living with likely incurable cancer, who often face barriers to accessing traditional mental health treatments.

Why it matters

Potential benefit: If successful, this study could provide a scalable and accessible treatment option for depression among cancer survivors.

How similar studies have gone: Previous studies have shown that evidence-based psychosocial treatments improve depression outcomes for cancer survivors, indicating potential success for this novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age \> 18 years
* ILLIC (as determined during manual chart review)
* Elevated depressive symptoms, defined as a score of ≥ 8 on the PHQ-9
* Current owner of an iOS- or Android-compatible smartphone
* Willingness to utilize a mobile app for the treatment of depressed mood (response of "yes" on yes/no item)
* Have a valid e-mail address that is checked regularly or have regular access to text messages (to access follow-up assessments)
* English language fluency

Exclusion Criteria:

* Current suicidal ideation at study screening, defined as a response greater than or equal to 1 on item nine of the PHQ-9
* Severe cognitive impairment that precludes completion of informed consent. For the purposes of assessing eligibility, this criterion is operationalized as:
* Prior diagnosis of dementia, or Major Neurocognitive Disorder indicated either via self-report or in the EHR; or
* Self-report of cognitive difficulties that impair functional independence

Where it's running

  • Medical University of South Carolina
    Charleston, South Carolina, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.