Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07227623

Randomized Trial of a Digital Health Intervention to Improve Physical Function and Wellness of Lung Cancer Survivors

Led by Massachusetts General Hospital · Updated on 2026-03-19

250

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

M

Massachusetts General Hospital

Lead Sponsor

A

American Cancer Society, Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a digital health intervention called PROMOTE to support lung cancer survivors undergoing treatment aimed at cure. The study focuses on people with stages I-III non-small cell lung cancer receiving chemotherapy with curative intent. It aims to improve physical function, manage breathlessness and sleep problems, increase physical activity, encourage healthy eating, and enhance overall wellbeing. The trial compares PROMOTE to enhanced usual care, including educational materials, to see which better supports survivors' health and quality of life. Participants will be randomly assigned to one of two groups: one receives the PROMOTE app delivered on a tablet, which includes educational modules and behavioral strategies for managing symptoms and improving lifestyle; the other group receives standard oncology care plus health education materials from the American Cancer Society. The intervention lasts about 10 to 12 weeks, during which participants use the app at their own pace alongside usual cancer treatment. Throughout the study, participants complete surveys at enrollment and at 6, 12, and 24 weeks to track changes in physical function, breathing difficulties, sleep disturbance, physical activity, diet, mood, and quality of life. The study also monitors participants' confidence in managing their health and coping skills. After 24 weeks, those in the control group will have the option to access the PROMOTE app. The total participation time spans about 24 weeks from enrollment to final assessment.

CONDITIONS

Brief Title

A Digital Health Intervention to Improve Physical Function and Wellness of Lung Cancer Survivors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with stage I-III non-small cell lung cancer
  • Within six weeks of starting curative treatment that includes chemotherapy, with or without immunotherapy, combined with surgery or chemoradiation
  • Eastern Cooperative Oncology Group Performance Status of 0 to 2 (fully active to ambulatory more than 50% of waking hours)
  • Able to use a digital health intervention with verbal and written information in English
  • Able to complete questionnaires in English or Spanish
  • Receiving primary cancer care at one of the participating institutions
Not Eligible

You will not qualify if you...

  • Having a significant uncontrolled psychiatric disorder or other co-morbid disease, such as dementia or cognitive impairment, that would prevent participation in study procedures as determined by the treating oncology clinician

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Approximately 10 weeks

Participants use the PROMOTE digital health app or receive enhanced usual care materials to improve physical function, manage symptoms, and enhance wellness during their lung cancer treatment.

Participants engage with the digital intervention modules at their own pace alongside standard oncology care

Follow-up

Duration - Up to 24 weeks post-enrollment

Participants complete self-report outcome measures to evaluate the impact of the intervention on physical function and other health outcomes.

3 visits for outcome assessments at 6, 12, and 24 weeks post-enrollment

Trial Site Locations

Total: 1 location

1

Massachusetts General Hospital

Boston, Massachusetts, United States, 02114

Actively Recruiting

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Research Team

J

Joseph A. Greer, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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