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About
The purpose of this study is to find out if it is practical to provide the program contained within the smartphone app AmDTx before and after lung cancer surgery. AmDTx is a platform that re-configures according to the specific needs of patients through physician prescriptions.
Enrollment
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Volunteers
Inclusion criteria
Histologically proven lung cancer
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
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
6 participants in 2 patient groups
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Central trial contact
Christian Nelson, PhD; Daniela Molena, MD
Data sourced from clinicaltrials.gov
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