Protocol No. | UW23133 23133 |
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Principal Investigator | Ward, Earlise | ||
Phase | N/A | ||
Age Group | Adult | ||
ClinicalTrials.Gov | NCT06472726 (Click to jump to clinicaltrials.gov) | ||
Management Group(s) | Palliative Care; UWCCC 1 South Park | ||
Title
Description
Objective
AIM 1. Adaptation of IONA Mind app for head and neck cancer. The research team will iteratively adapt the IONA Mind app to provide psychological support for HNC patients and survivors. The HNC Survivors Advisory Board will assist in identifying key aspects of the HNC survivors' journey from diagnosis to the survivorship phase, which will be prioritized and considered to iteratively redesign the IONA Mind phone app to better support HNC patients and survivors AIM 2. Identify feasibility of the IONA Mind app for head and neck cancer. The IONA Mind app will be tested with 30 HNC patients and survivors, recruited from the Survey of the Health of Wisconsin (SHOW) recruitment registry and from the clinical practice at UW Carbone Cancer Center (UWCCC) AIM 3. Determine preliminary efficacy IONA Mind app tailored for depression comorbid with head and neck cancer. Clinical outcomes will be measured at baseline, weekly for 6 weeks (including the 6-week period of app utilization), and post-intervention follow-up conducted at 1- and 3-month post intervention using validated tools to access depression AIM 4. Determine satisfaction and acceptability of the IONA Mind app. Satisfaction with the IONA Mind app will be measured with the System Usability Scale (SUS) delivered at 1-2 weeks following the completion of the app utilization. In addition, a qualitative interview for a random sub sample of 10 - 15 participants will occur shortly after completion of the intervention to assess satisfaction with and acceptability of the mobile app. A head and neck patient and survivor phone app Low-Intensity Cognitive Behavioral Therapy (LiCBT) intervention to treat depression co-designed by HNC advocates, mental health professionals and an expert technologist is a critical outcome of this research.
Treatment
This study is being done to estimate the feasibility/efficacy/acceptability of the IONA Mind app for head and neck cancer (HNC) patients and survivors who show evidence of comorbid depression.
Key Eligibility
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 >/= 10 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
Applicable Disease Sites
Participating Institutions
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