App for cancer depression fails to launch: trial ends after just one participant
NCT ID NCT06472726
First seen Jun 27, 2026 · Last updated Jul 31, 2026 · Updated 2 times
Summary
This study aimed to see if a smartphone app called IONA Mind could help treat depression in people who have had head and neck cancer. Participants would use the app for 6 weeks and fill out surveys. However, the trial was terminated early after enrolling only 1 person, so no meaningful results were obtained.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- IONA Mind app (a smartphone app for mental health support)
- What this could lead to
- If it worked, this could point toward a convenient, app-based way to ease depression in head and neck cancer survivors.
- What could go wrong
- The trial was terminated after enrolling only 1 person, so we have almost no data. It is too early to know if the app helps or is even usable in this group.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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1 person
The number who actually took part.
- Started
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Jul 2025
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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22 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * History of HNC confirmed by histopathologic diagnosis. The signed report must be available on electronic health record (EHR) for participants who received treatment or follow-up at University of Wisconsin Carbone Cancer Center (UWCCC). Alternatively, participants must have a printed signed report if received treatment out of UWCCC * Age greater than or equal to 22 years at the time of consent * Patient Health Questionnaire-9 (PHQ-9) score ≥ 5 and ≤ 19 (moderate and severely moderate depression) * Willing to comply with all study procedures and be available for the duration of the study. Exclusion Criteria: * Unable to read and speak English. * Utilization of prescription medicine for depression. * Patient Health Questionnaire-9 (PHQ-9) score of greater than or equal to 20 (severe depression) * Patient Health Questionnaire-9 (PHQ-9) score greater than or equal to 1 on the suicidal question (question 9) * Pregnant people
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Wisconsin Carbone Cancer Center
Madison, Wisconsin, 53705, United States
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