Active Not RecruitingNot applicableNCT06008574

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

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.

Checked against the public recordLast updated Sep 17, 2025 · Source: ClinicalTrials.gov

StatusActive Not Recruiting
PhaseNot applicable
U.S. locations7
SponsorMemorial Sloan Kettering Cancer Center
01
Study overview

What this study is about

Purpose
Supportive Care
Study type
Interventional
Phase
Not applicable
Sponsor
Memorial Sloan Kettering Cancer Center
Interventions being studied
Other: AmDTx-PCSP; Other: AmDTx-2048; Other: Questionnaires
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Treatment approach
03
Public criteria

Who may be able to participate

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 Exclusion Criteria: * Currently engaging in app-based mindfulness or meditation for one or more times per week * As per self-report or as documented in the medical record, current untreated (e.g., no medication, no therapy) major psychotic disorder (schizotypal personality disorder, schizophreniform disorder, schizoaffective disorder). Patients diagnosed with a major psychiatric disorder will be reviewed by the study PI to determine eligibility before consent * Individuals with impaired decision-making capacity * Patients that need to undergo neoadjuvant therapy (chemotherapy±radiation) * Patients undergoing active treatment of other non-lung cancers * Patients with recurrent lung cancer

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Memorial Sloan Kettering Basking Ridge (All Protocol Activities)Basking Ridge, New Jersey
  • Memorial Sloan Kettering Monmouth (All Protocol Activities)Middletown, New Jersey
  • Memorial Sloan Kettering Bergen (All Protocol Activities)Montvale, New Jersey
  • Memorial Sloan Kettering Suffolk - Commack (All Protocol Activities)Commack, New York
  • Memorial Sloan Kettering Westchester (All protocol activities)Harrison, New York
  • Memorial Sloan Kettering Cancer Center (All Protocol Activities)New York, New York
  • Memorial Sloan Kettering Nassau (All Protocol Activities)Rockville Centre, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Sep 17, 2025. Always confirm current availability with the study team.

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