CompletedNot applicableNCT05014035

Feasibility of a Hybrid Delivery of Home-based Cluster Set Resistance Training in Lung Cancer

Symptom burden remains a critical concern for individuals with non-small cell lung cancer (NSCLC) following the completion of treatment. Of those, symptom clusters such as dyspnea (shortness of breath) and fatigue, contribute to physical decline, reductions in quality of life, and a higher risk of comorbidities and mortality. It has been proposed that dyspnea is a primary limiter of exercise capacity in individuals with lung cancer, resulting in exercise avoidance and an accelerated physical decline. As such, specifically designing resistance exercise programs with cluster sets, to mitigate feelings of dyspnea and fatigue may result in improved exercise tolerance, resulting in the maintenance of physical function and quality of life. The purpose of this project is to investigate the feasibility and preliminary efficacy of a hybrid-delivery of home-based cluster-set resistance exercise in individuals with NSCLC. Methods: Individuals with NSCLC (n=15), within 12-months of completion of treatment will be recruited to participate in this single arm feasibility trial. Participants will complete 8-weeks of home-based resistance training (RT) designed to target dyspnea and fatigue. The hybrid-delivery of the program will include supervised sessions in the participants home, and virtual supervision via video conferencing. The primary outcome of feasibility will be measured via recruitment rates, retention, acceptability and intervention fidelity. Exploratory outcomes (dyspnea, fatigue, quality of life, physical function and body composition) will be assessed pre- and post- intervention.

Checked against the public recordLast updated May 12, 2023 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations1
SponsorUniversity of South Carolina
01
Study overview

What this study is about

Purpose
Other
Study type
Interventional
Phase
Not applicable
Sponsor
University of South Carolina
Interventions being studied
Behavioral: Resistance Exercise
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

Inclusion Criteria: * Completed definitive treatment for localized NSCLC (stages I-III) * Has access to stable internet access for Zoom participation * Willing to complete an 8-week, home-based intervention program that includes face-to-face and Zoom interaction. * Willing to consider behavior change at this time. * Able to speak and read English. * Capable of informed consent * Has obtained medical clearance from medical practitioner or medical team Exclusion Criteria: * Individuals with a known diagnosis of advanced lung cancer (stage IV; due to potential added burden) or diagnosis of small-cell lung cancer, * Anyone for whom physical activity is not recommended. * aren't comfortable having study staff visit their homes for exercise sessions * have any neuromuscular, cardiovascular, or psychological condition precluding safe exercise; * have participated in structured RE ≥2 times/week for the past 6 months; * are unable to read/understand English.

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 South CarolinaColumbia, South Carolina

Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 12, 2023. Always confirm current availability with the study team.

View original record ↗