A Study Comparing Mindfulness Apps to Decrease Anxiety in People With Lung Cancer

Inclusion Criteria

• •Histologically proven lung cancer
• •* Patients with suspected primary lung cancer per recent chest CT scan (with or without contrast) may be enrolled in the trial. These patients may be randomized and begin study intervention without a biopsy. If a patient undergoes a biopsy after consent and the results are negative or if the patient does not proceed with surgery, the patient will be removed from the study. The patient will continue to receive full access to the AmDTx app for 2-years.
• •* Scheduled for surgery with at least 14 days lead time (to allow the participant to start the mindfulness practice \[intervention group\] 14 days preoperatively)
• •Age ≥18 years of age at time of signing informed consent
• •Access to a smartphone/tablet with data connection
• •Willing to give time for mindfulness practice (Patients need to have the motivation to devote approximately 20 to 30 min daily, which is equal to 5 to 7 sessions a week over the course of a minimum of 6 weeks to do the mindfulness meditations and practices)
• •Willing to be randomized to mindfulness MBCR or CI group and complete all assessments
• •High distress level (Distress Thermometer score ≥4 at initial visit)
• •Able to understand the study objectives and procedures, comply with the protocol, and sign an informed consent
• •Able to read, speak, and understand English