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NCT07498972Completed

Evidence-Based Nursing Plus Progressive Exercise for Cancer-Related Fatigue in Advanced Lung Cancer

Effect of Evidence-Based Nursing Combined With Progressive Gymnastics Training on Cancer-Related Fatigue, Quality of Life, and Treatment Adherence in Patients With Advanced Lung Cancer Undergoing Chemotherapy: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

This study aims to evaluate the effectiveness and safety of evidence-based nursing combined with progressive exercise training in patients with advanced lung cancer undergoing chemotherapy. Cancer-related fatigue (CRF) is a common and distressing symptom in this population and is associated with poor quality of life and reduced treatment adherence. In this single-center, prospective randomized controlled trial, 100 patients with stage III-IV lung cancer receiving platinum-based chemotherapy were randomly assigned to either a control group or an intervention group. The control group received routine nursing care, while the intervention group received evidence-based nursing combined with a structured progressive exercise program for 8 weeks. The primary outcomes are cancer-related fatigue assessed by the Brief Fatigue Inventory (BFI) and functional exercise capacity assessed by the 6-minute walk test (6MWT). Secondary outcomes include quality of life (EORTC QLQ-C30), treatment adherence (MMAS-8), psychological status (HADS), sleep quality (PSQI), and safety outcomes. The study is designed to determine whether a combined intervention approach integrating nursing care and exercise rehabilitation can provide greater benefits than routine care alone in improving both physical and psychological outcomes in patients with advanced lung cancer.

Status (registry)
Completed
Study type
Interventional
Enrollment
100 (actual)
First submitted
18 Mar 2026
Start date
1 Jan 2023
Primary completion date
30 Jun 2024
Lead sponsor
Shanxi Province Cancer Hospital
Diseases
Lung cancer
NCT number
NCT07498972

What you commit to

  • Study type: Interventional
  • Participants enrolled: 100
  • From 1 Jan 2023 to the primary completion date, 30 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Severe cardiopulmonary insufficiency or other conditions that contraindicate exercise intervention
  • Cognitive impairment or mental disorders affecting compliance with the intervention
  • Musculoskeletal disorders that limit physical activity or exercise participation
  • Presence of other advanced malignant tumors
  • Rapid disease progression during the study period requiring discontinuation of the intervention

Who the study is looking for

  • Pathologically confirmed advanced lung cancer (stage III-IV)
  • Currently receiving platinum-based chemotherapy (first to fourth cycle)
  • Age ≥18 years
  • Karnofsky Performance Status (KPS) score ≥60
  • Presence of moderate or more severe cancer-related fatigue, defined as a Brief Fatigue Inventory (BFI) score ≥4
  • Expected survival time of more than 6 months
  • Ability to understand the study procedures and provide written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Shanxi Province Cancer Hospital
Coordinator of this site? Confirm its status
TaiyuanChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.