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Artificial Intelligence-Powered Support For Quality Of Life Improvement In Participants With Cancer

Artificial Intelligence-Powered Support For Quality Of Life Improvement In Patients With Cancer

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07167056
Enrollment
60
Registered
2025-09-11
Start date
2025-11-17
Completion date
2027-01-15
Last updated
2025-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Psychotherapy, Mental health, Distress, Stage I Cancer, Stage II Cancer, Stage III Cancer, Chatbot, Artificial Intelligence, AI

Brief summary

This research study is for people who are diagnosed with cancer and are receiving treatment for cancer who may benefit from psychotherapy. The purpose of the study is to see whether an artificial intelligence (AI) powered application (app) could help improve quality of life, anxiety symptoms, and/or depression symptoms, over the course of psychotherapy sessions. Participants in this study will be randomly assigned to one of two groups. One group will receive psychotherapy per usual care and will receive access to the AI-powered app. The second group will only receive psychotherapy per usual care and will NOT receive access to the AI-powered app. Both groups will complete surveys about their quality of life, anxiety symptoms, and depression symptoms over the course of their psychotherapy visits.

Detailed description

Getting a cancer diagnoses and going through treatment can be difficult and lead to symptoms of distress, like anxiety and depression. Feeling distressed or upset can make people with cancer feel worse and potentially shorten how long they live. Because of this, it is important to address the distress that people with cancer may feel in order to improve their well-being. Treatments that don't use medication, like psychotherapy (talk therapy), relaxation techniques, and mindfulness, can help reduce distress in people with cancer. However, some people do not have access to these types of things, and mental health care overall can be limited by financial, logistical, and geographical barriers. One solution to these barriers could be artificial intelligence (AI)-powered interventions using mobile applications (apps) on someone's phone. AI tools, like chatbots, can provide personal support. They can use Cognitive Behavioral Therapy (CBT) and mindfulness to provide support. They can also provide tools to track someone's mood. AI tools do not replace a diagnosis from a doctor or treatment from a doctor or other clinical care provider. However, these tools could still support and help to improve someone's mental health and well-being. People who have studied this have found that this day-to-day support has decreased anxiety and depression in the general population. However, the use of AI tools to support mental health in people with cancer is not yet well studied. WYSA is an AI-powered chatbot that uses evidence-based techniques like Cognitive Behavioral Therapy (CBT) and mindfulness. For the purposes of this study, WYSA will be used in addition to standard of care psychotherapy. WYSA will not replace psychotherapy care in this study, and it will not replace a doctor's advice or diagnoses.

Interventions

Participants will receive six psychotherapy sessions over the course of approximately 3 months.

BEHAVIORALWYSA App

Participants will have access to the WYSA mental health support artificial intelligence app over the course of the 3 months that they are participating in psychotherapy sessions per standard of care. The app will contain features intended to manage symptoms of depression and anxiety in individuals with cancer. The app will include an AI-powered chatbot with Cognitive Behavioral Therapy (CBT) and mindfulness techniques, visual progress elements (a progress roadmap, a weekly progress report, etc.), and a customizable tool library. Participants are instructed to use the app whenever they feel like it, if they are in distress, or if the app prompts them to use it. App prompts (notifications) will occur once daily.

Sponsors

Florida Department of Health (Casey DeSantis Florida Cancer Innovation Fund)
CollaboratorUNKNOWN
Case Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participants in active cancer treatment (receiving chemotherapy, immunotherapy and/or radiation therapy) AND reporting National Comprehensive Cancer Network (NCCN) Distress Thermometer scores ≥4. The NCCN Distress Thermometer is a validated, single-item screening tool routinely used in cancer care at Cleveland Clinic Florida to identify individuals experiencing psychological distress. A score of 4 or higher indicates clinically significant distress and serves as the eligibility threshold for enrollment in this study. * Participants followed by a medical oncologist, radiation oncologist, and/or surgical oncologist of any subspecialty at Cleveland Clinic Florida and have no barrier to receive psychotherapy care (e.g. no insurance restrictions) * Participants with biopsy proven cancer of any type, stages I-III. * Adults aged 18 years or older. * Able to understand and read English and/or Spanish. * Participants who own a smartphone compatible with the mobile app (Android or IOS) or have regular (Daily) access to one. * Participants who are willing and able to provide informed consent.

Exclusion criteria

* Age \<18 years. * Participants with stage 4 cancer. * Participants with active severe psychiatric conditions identified by the Cleveland Clinic psychotherapist as any diagnoses that could significantly impair a participant's ability to engage meaningfully with the intervention or provide informed consent. These include, but are not limited to: * Current or recent (within the past 6 months) psychotic disorders (e.g., schizophrenia, schizoaffective disorder) * Bipolar disorder in a manic or severe depressive phase * Active suicidal ideation with intent or recent suicide attempt (within the past 6 months) * Severe cognitive impairment or neurocognitive disorders that compromise comprehension or communication or interferes with chatbot use. * Any condition requiring psychiatric hospitalization within the past 6 months * Concurrent enrollment in another trial targeting psychological distress to avoid bias. * Limited life expectancy (\<3 months) as determined by the oncologist.

Design outcomes

Primary

MeasureTime frameDescription
Change in Quality of LifeBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.

Secondary

MeasureTime frameDescription
Change in DepressionBaseline, 3 monthsDepression is measured by the Patient Health Questionnaire-9 (PHQ-9). The PHQ-9 contains 8 questions asking participants about their depression symptoms on a 4-point Likert scale from Not at all (0) to Nearly every day (3). There is one questions regarding how difficult these symptoms have made daily life, where participants provide an answer on a 4-point scale from Not difficult at all to Extremely difficult. Higher scores indicate greater depression symptoms.
Change in physical functioningBaseline, 3 monthsPhysical functioning is measured by the physical functioning (functional scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains five questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate lower physical functioning.
Change in role functioningBaseline, 3 monthsRole functioning is measured by the role functioning (functional scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains two questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate lower role functioning.
Change in emotional functioningBaseline, 3 monthsEmotional functioning is measured by the emotional functioning (functional scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains four questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate lower emotional functioning.
Change in cognitive functioningBaseline, 3 monthsCognitive functioning is measured by the cognitive functioning (functional scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains two questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate lower cognitive functioning.
Change in social functioningBaseline, 3 monthsSocial functioning is measured by the social functioning (functional scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains two questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate lower social functioning.
Change in fatigueBaseline, 3 monthsFatigue is measured by the fatigue (symptom scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains three questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater fatigue symptoms.
Change in nausea/vomitingBaseline, 3 monthsNausea/vomiting is measured by the nausea and vomiting (symptom scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains two questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater fatigue symptoms.
Change in painBaseline, 3 monthsPain is measured by the pain (symptom scale) subscale of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It contains two questions, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater fatigue symptoms.
Change in dyspneaBaseline, 3 monthsDyspnea is measured by the dyspnea (symptom item) item of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It is one question, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater dyspnea symptoms.
Change in insomniaBaseline, 3 monthsInsomnia is measured by the insomnia (symptom item) item of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It is one question, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater insomnia symptoms.
Change in appetite lossBaseline, 3 monthsAppetite loss is measured by the appetite loss (symptom item) item of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It is one question, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater appetite loss symptoms.
Change in constipationBaseline, 3 monthsConstipation is measured by the constipation (symptom item) item of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It is one question, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater constipation symptoms.
Change in diarrheaBaseline, 3 monthsDiarrhea is measured by the diarrhea (symptom item) item of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It is one question, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater diarrhea symptoms.
Change in financial difficultiesBaseline, 3 monthsFinancial difficulties is measured by the financial difficulties (symptom item) item of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) version 3.0 questionnaire. It is one question, where participants provide an answer on a 4-point Likert scale from Not at all (1) to Very Much (4). Higher scores indicate greater financial difficulties.
Engagement, measured by frequency of use of appLength of participation, up to 3 monthsFrequency will be measured by the amount of times that participants use the app, recorded as the date/time of usage
Engagement, measured by tool usage in appLength of participation, up to 3 monthsThe app contains tools related to mindfulness and Cognitive Behavioral Therapy (CBT)-informed approaches. Engagement is measured by frequency of tool usage.
Change in AnxietyBaseline, 3 monthsAnxiety is measured by the Generalized Anxiety Disorder-7 (GAD-7) questionnaire. The questionnaire contains 7 questions asking participants about their anxiety symptoms on a 4-point Likert scale from Not at all (0) to Nearly every day (3). There is one questions regarding how difficult these symptoms have made daily life, where participants provide an answer on a 4-point scale from Not difficult at all to Extremely difficult. Higher scores indicate greater anxiety symptoms.
Incidence of adverse events (AEs)One month after completion of participation, up to 4 months
Change in Quality of Life, according to number of psychotherapy visits completedBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of genderBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of raceBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of ethnicityBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of marital statusBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of cancer typeBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of cancer stageBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of time since diagnosisBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of comorbiditiesBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of insurance statusBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of in-person vs virtual psychotherapy visitBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of current therapy regimenBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of current psychiatric medicationBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of current mental health diagnosisBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Change in Quality of Life, according to participant characteristic of number of psycho-oncology visits attended previouslyBaseline, 3 monthsQuality of life (QoL) is measured by the global health status/QoL subscale of the EORTC QLQ-C30 version 3.0 questionnaire. The global health status/QoL subscale contains two questions, where participants provide an answer on a 7-point Likert scale from Very poor (1) to Excellent (7). Higher scores indicate greater global health status/QoL.
Engagement, measured by length of app chatbot interactionLength of participation, up to 3 monthsLength is defined as number of messages exchanged during chatbot interaction.

Countries

United States

Contacts

Primary ContactZeina Nahleh, MD, FACP
nahlehz@ccf.org954-659-5840

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026