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NCT07214441

Evaluating the Feasibility and Preliminary Effects of BE+

Enrolling by Invitation
NAAges 21+InterventionalSupportive care
University of South Carolina
~20 participants
Updated 2025-10-09 on ClinicalTrials.gov
What's tested:Breathe Easier+

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Evaluate the feasibility of the 12-week BE+ (BE with RT) among NSCLC survivors and their partners (dyads).
Measured over 12 weeks

Conditions

Lung Cancer (Non-Small Cell)
Self-management Behavior
Physical Activity
Stress
Quality of Life
Resistance Training

Explore related trials

Lung Non-Small Cell Carcinoma

Where it's being run

1 sites across 1 states
South Carolina1

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

Survivors of NSCLC who have completed definitive treatment within the last 2 years.
All participants must have a health clearance for physical activity signed by a healthcare provider; have Wi-Fi access; be able to provide informed consent; and be able to speak and read English.

Exclusion

Survivors on current definitive treatment.
All participants with a history of recurrent falls; a substantial mobility impairment related to chronic disease or injury; and lack of physical activity readiness as determined by a healthcare provider.

What this trial measures

  • Evaluate the feasibility of the 12-week BE+ (BE with RT) among NSCLC survivors and their partners (dyads).12 weeks

    Feasibility will be evaluated on: 1. Enrollment (25% of eligible participants), 2. Retention (80% of participants at study completion), 3. Adherence (80% to complete instruments at time points 1-3; Fitbit wear \>5 days each week for 12 weeks), 4. Participation (80% to log physical activity weekly, log breathing exercises weekly, set goals weekly, attend 2 resistance training sessions weekly, participate in weekly phone call, and read daily text messages),