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N/A N=235 Randomized Other

Understanding the Post-Surgical Non-Small Cell Lung Cancer Patient's Symptom Experience

Fatigue · Self Efficacy · Quality of Life · Physical Activity · Lung Cancer

Enrolled (actual)
235
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcome: Primary: Cancer-related Fatigue Severity Using The Brief Fatigue Inventory. — 0.56; 4.19; 4.93 Scores on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Light Physical Activity 1 (Behavioral); Light Physical Activity 2 (Behavioral); Support Education Activity (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Nebraska
Primary completion
Nov 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Cancer-related Fatigue Severity Using The Brief Fatigue Inventory.
0.56; 4.19; 4.93
PRIMARY
Cancer-Related Fatigue Fatigability as Assessed Using the 6 Minute Walk Test.
389; 312; 300
SECONDARY
Other Symptoms Severity
0.81; 1.57; 1.93
SECONDARY
Perceived Self-Efficacy for Fatigue Self-Management
9.39; 6.31; 5.3
SECONDARY
Self-Efficacy for Walking Duration
7.99; 5.15; 4.59
SECONDARY
Activities-Specific Balance Confidence
9.1; 8; 7.54
SECONDARY
Steps Per Day
3939; 3620; 2802
SECONDARY
Functional Status Performance
45.97; 39.51; 35.57
SECONDARY
Quality of Life as Assessed Using the Quality of Life Index
24.98; 23.61; 21.92

Summary

Among 13 core symptoms across 3,106 breast, colorectal, prostate, and lung cancer patients, persons with lung cancer were the most symptomatic, with moderate to severe fatigue being reported with the greatest prevalence. This is a proposed randomized controlled trial of a novel rehabilitative intervention for persons with non-small cell lung cancer after surgery that promotes self-management of cancer-related fatigue (CRF) and is practical, portable, low cost, and safe. The results of the study will provide a novel exercise intervention, and its optimal timing, that helps a vulnerable population by reducing CRF severity and fatigability and is applicable to nearly all post-thoracotomy lung cancer patients.

Eligibility Criteria

Inclusion Criteria

  • Women and men
  • At least 18 years of age (Michigan) and 19 years of age in (Nebraska)
  • With suspected non-small cell lung cancer to be confirmed after surgery
  • Karnofsky Performance Status score of at least 70%
  • Thoracic surgeon approval pre- and post-surgery
  • Medically stable comorbid conditions allowing for non-small cell lung cancer surgery clearance
  • Has phone access capability
  • Able to speak and write English
  • Able to hear and speak for phone interviews
  • Owns a television
  • Lives within 2 hours driving distance of recruitment site

Exclusion Criteria

  • Severe impairment of sight, hearing, speaking
  • Active treatment for malignancy within past 3 months (other than non-melanoma skin cancer or long-term hormonal treatment for common cancers such as breast and prostate if disease is stable
  • Weight greater than 330 pounds
  • History of photosensitive seizures
  • Any condition or disorder that would impede safe participation as directed
  • Plans to relocate outside the area during the study period or unable to fully participate
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03724331). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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