Phase II Pilot Study Evaluating the Feasibility of Delivery and Evaluation of a Digital Cognitive-Behavioral Stress Management (CBSM) Device (BNT001) for Treatment of Anxiety and Depressive Symptoms in Patients With Stage I-III Breast or Stage I-III Non-Small Cell Lung Cancer
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Anatomic Stage I Breast Cancer AJCC v8
- Sponsor
- Jonsson Comprehensive Cancer Center
- Enrollment
- 5
- Locations
- 1
- Primary Endpoint
- Feasibility of implementing and evaluating the BNT001 digital Cognitive-Behavioral Stress Management device
- Status
- Terminated
- Last Updated
- 2 years ago
Overview
Brief Summary
This phase II trial studies the effect of a digital application (app), BNT001, on cognitive-behavioral stress management in patients with stage I-III breast or lung cancer. The app is designed for cancer patients to treat anxiety and depressive symptoms related to their cancer diagnosis. The purpose of this study is to develop and refine procedures for eligibility screening, suicide risk assessment, and delivery of the app prior to the launch of a phase III randomized trial. The impact of the app in managing stress and improving quality of life and mood is a secondary aim.
Detailed Description
PRIMARY OBJECTIVE: I. To assess the feasibility of implementing and evaluating a digital cognitive-behavioral stress management (CBSM) device, BNT001, in stage I-III breast or stage I-III non-small cell lung cancer currently undergoing treatment or recently completed treatment (\< 3 months). SECONDARY OBJECTIVES: I. To collect preliminary data regarding the efficacy of the intervention with regard to improvements in patients' reported symptoms of distress. II. To evaluate patient safety and risks associated with screening procedures (severe anxiety or depression) as well as during receipt of the digital intervention. OUTLINE: Prior to participating in the study patients complete an online baseline questionnaire to assess anxiety and depression and general quality of life, as well as some specific questions related to their coping. They are also interviewed by a clinician who rates their level of anxiety and depression. After this, patients use the BNT001 app and undergo 10 sessions of CBSM over 45-60 minutes each consisting of cancer-specific educational videos, guided relaxation training, interactive exercises, and discussion modules. Following completion of the 5th session, patients undergo a telephone check-in assessment to see how things are going, update their treatments and medications, and schedule a phone call to assess for adverse events. At the end of the 10th session, patients complete a post-treatment online questionnaire and a phone debriefing interview to discuss their experience with the intervention.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age 18 years or older
- •Diagnosis of stage I-III breast cancer or stage I-III non-small cell lung cancer
- •Currently in active treatment or have completed initial cancer directed treatments (surgery, radiation, chemotherapy) within the past 3 months
- •Patients showing moderate anxiety (General Anxiety Disorder-7 Questionnaire \[GAD-7\] \> 10) or mild depression (Patient Health Questionnaire depression scale \[PHQ-8\] score 5-11)
- •Fluent in English
- •Has access to smartphone or tablet capable of running iOS or Android software
Exclusion Criteria
- •Previous history of cancer
- •\< 2-year (yr) survival prognosis
- •Endorses thoughts of self-harm on question 9 of the Patient Health Questionnaire-9 (PHQ-9) (any score \> 0)
- •Currently participating in investigative behavioral intervention trial for treatment of anxiety or depression
- •Participant is unable to complete training, cognitive deficits, major psychiatric conditions, psycho-social conditions; lack of access to internet accessible device; other social conditions that would interfere with adherence to self-directed care, such that in investigator's opinion the participant would be unable to complete the study
- •Recently completed use of Blue Note Therapeutics COVID Cancer Care Program or other Blue Note Therapeutics-sponsored study
- •Planning to seek other psychosocial support services while participating in this study
Outcomes
Primary Outcomes
Feasibility of implementing and evaluating the BNT001 digital Cognitive-Behavioral Stress Management device
Time Frame: Up to 1 year
Feasibility will be evaluated by the rate of recruitment, total number of screens and number of screen fails, treatment adherence (as measured on the backend based on time and regularity of engaging with the digital platform), and number of study completers versus enrolled. The analytic strategy will be primarily descriptive and qualitative. Will also obtain qualitative feedback on participation in the study and study intervention through the end of study de-briefing interview.
Secondary Outcomes
- Change in depression symptoms(Baseline up to 10 weeks)
- Change in global health(Baseline up to 10 weeks)
- Change in anxiety symptoms(Baseline up to 10 weeks)
- Patient safety and risks(Up to 10 weeks)
- Change in anxiety(Baseline up to 10 weeks)
- Change in depression(Baseline up to 10 weeks)