WithdrawnNot applicableNCT04318249
Official study title

Behavioral Relaxation Approaches for Insomnia in Lung Cancer Patients

Study summary

This is a randomized, 30-day research study that is exploring the effects of two simplified mindfulness interventions in lung cancer patients aimed to improve their sleep quality and anxiety regarding sleep. The investigators will be enrolling a total of 20 patients who have insomnia symptoms. Patients will use a behavioral intervention to help with their sleep.

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Key things to know

Main goalTreatment

This describes the study’s primary purpose.

What is being studiedAssisted Relaxation Therapy and Modified Assisted Relaxation Therapy

The study team can explain what participation involves.

Who it may be forInsomnia

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Nov 25, 2024 · Source: ClinicalTrials.gov

Is enrollment open?Withdrawn

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Interventional

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?Abramson Cancer Center at Penn Medicine

Study sponsor

01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Not applicable
Sponsor
Abramson Cancer Center at Penn Medicine
Interventions being studied
Behavioral: Assisted Relaxation Therapy; Behavioral: Modified Assisted Relaxation Therapy
02
Explore related studies

How this study is categorized

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

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • 18 or older
  • Diagnosed with Lung Cancer (In remission, Undergoing Immune Modulated Chemotherapy, Undergoing Platinum-based Chemotherapy
  • Fluent in English
  • Has Access to Smartphone
  • Has internet connection at home
  • More than 4 weeks post-surgery
Reasons someone may not be able to joinExclusion criteria
  • Inability to speak English or communicate verbally
  • Medical or other factors that, in the opinion of the study research team, would interfere with their ability to participate in the intervention (such as inability to participate in the guided compassion training due to deafness)

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

  • University of PennsylvaniaPhiladelphia, Pennsylvania

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Nov 25, 2024. Always confirm current availability with the study team.

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