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NCT01937637 · ClinicalTrials.gov registry record · NA

Improving Management of Breathlessness in Patients With Lung Cancer

A NA study of Lung Cancer and Dyspnea, sponsored by Massachusetts General Hospital.

Completed
Registry status
NA
Development phase
32
Enrollment target
1
Study location

NCT01937637: Completed NA study of Lung Cancer and Dyspnea, sponsored by Massachusetts General Hospital.

NCT01937637 is a NA study of Lung Cancer and Dyspnea that has completed, run by Massachusetts General Hospital. The registered enrollment target is 32 participants, below the 936-participant average among 409 other Lung Cancer trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01937637, a NA study of Lung Cancer and Dyspnea, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
NA
Development phase
32 participants
Enrollment target
1
Study location

Study Summary

Many individuals with lung cancer experience debilitating breathlessness at some point during the course of their illness. Unfortunately, few interventions exist to treat this distressing symptom of cancer. In this study, the investigators plan on recruiting individuals with lung cancer to participate in a behavioral intervention to help relieve breathlessness. The principal investigator of the study, Dr. Joseph Greer, is a licensed clinical psychologist who has trained nurse practitioners in how to deliver the behavioral intervention. The nurse practitioners will meet with patients diagnosed with lung cancer during their outpatient oncology appointments, such as chemotherapy infusions, to review the behavioral skills that may help with breathlessness. Specifically, the intervention includes education about the relationship between breathlessness and the stress response as well as teaches patients skills for breathing control and relaxation of the body. For this single-group pilot study, the investigators will ask participants to provide feedback about whether they found the intervention acceptable and effective. Participants will also complete questionnaires about their physical and psychological symptoms before and after the intervention in order to measure its effectiveness for treating breathlessness and any distress related to breathlessness. The data from this study will help inform improvements to the intervention in order to make it feasible and effective for treating breathlessness in patients with lung cancer.

Primary Outcome

Feasibility and acceptability of the intervention will be determined via individual qualitative, exit interviews with participants. These interviews will assess the following: 1) satisfaction with the dyspnea intervention; 2) perceptions of potential problems with the approach, and 3) recommendations for improving the dyspnea intervention and delivery methods to enhance feasibility and acceptability.

Interventions

  • BEHAVIORAL Cognitive Behavioral Intervention for Breathlessness

Study Locations (1)

Massachusetts

  • Massachusetts General Hospital - Boston

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2013-07
Est. Completion 2014-11
Phase NA
Massachusetts General Hospital

2,032 total trials

What the finished NCT01937637 record still lists

NCT01937637 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 936-participant average among 409 other Lung Cancer trials with a reported enrollment target (97% lower).

The record links to 3 conditions, with Lung Cancer appearing as the primary indexed condition, and to 1 intervention - of which Cognitive Behavioral Intervention for Breathlessness is the first listed.

NCT01937637 reports a single indexed study location in Massachusetts.

Frequently Asked Questions

What is clinical trial NCT01937637 about?

NCT01937637 is a clinical study titled "Improving Management of Breathlessness in Patients With Lung Cancer". Many individuals with lung cancer experience debilitating breathlessness at some point during the course of their illness. Unfortunately, few interventions exist to treat this distressing symptom of cancer. In this study, the investigators plan on recruiting individuals with lung cancer to particip...

What is the current status of trial NCT01937637?

This trial is currently completed. It is a NA study. The enrollment target is 32 participants. The study started on 2013-07. Estimated completion is 2014-11.

What conditions does trial NCT01937637 study?

This clinical trial studies the following conditions: Lung Cancer, Dyspnea, Breathlessness.

What interventions are being tested in trial NCT01937637?

The interventions under investigation include: Cognitive Behavioral Intervention for Breathlessness (BEHAVIORAL).

Who is sponsoring clinical trial NCT01937637?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01937637 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lung Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01937637's enrollment target sits among peer trials

32 314th of 409 higher than 94 of 409 other Lung Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Lung Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01937637, the US trial registry maintained by the National Library of Medicine. NCT01937637 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.