Identification of Changes in Cancer-related Fatigue and Physical Activity and Their Association in Patients With Inoperable Lung Cancer: a Longitudinal Observational Study (AcTiF)
16. September 2026 aktualisiert von: University Hospital, Ghent
The goal of this observational study is to learn how fatigue changes during lung cancer treatment and how it relates to physical activity levels in adults with locally advanced, inoperable, or metastatic lung cancer who are starting chemotherapy and/or immunotherapy. The main questions to answer are:
- How do fatigue and physical activity levels change throughout lung cancer treatment?
- How are changes in fatigue related to physical activity levels on the short- and long term?
Participants will:
- Complete questionnaires on fatigue, breathlessness, sleep quality, quality of life, stress, anxiety and depression at multiple time points.
- Wear activity monitors during four measurement periods to assess daily physical activity.
- Complete brief daily smartphone questionnaires on fatigue, breathlessness, pain, and perceived ability to walk.
- Wear a smartwatch throughout the study.
- Undergo physical assessments, including a 1-minute sit-to-stand test, a thigh muscle strength test, and a frailty assessment.
- Attend six study visits over the course of the study, some of which may be scheduled alongside routine hospital appointments.
Studienübersicht
Status
Rekrutierung
Studientyp
Beobachtungs
Einschreibung (Geschätzt)
50
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Oost-Vlaanderen
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Ghent, Oost-Vlaanderen, Belgien, 9000
- Rekrutierung
- UZ Gent
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Kontakt:
- Francesca Van Hulle, Msc.
- Telefonnummer: +32470577042
- E-Mail: francesca.vanhulle@ugent.be
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Nein
Probenahmeverfahren
Nicht-Wahrscheinlichkeitsprobe
Studienpopulation
This study will include patients with locally advanced irresectable or metastatic lung cancer, who are planned to undergo systemic treatment (chemotherapy and/or immunotherapy).
Beschreibung
Inclusion Criteria:
- Locally advanced irresectable or metastatic lung cancer (all histologies including NSCLC and SCLC).
- ≥18 years.
- ECOG performance status of ≤2 (a lower score indicates a higher performance status), assessed by the clinician (10).
- Planned to start a first-line systemic treatment consisting of chemotherapy and/or immunotherapy. Patients who receive radiotherapy, concurrently or sequentially, within a multimodality treatment approach for locally advanced lung cancer are allowed.
- Ability to give informed consent.
Exclusion Criteria:
- Being planned for primary radiotherapy with radical intent only or treatment with targeted therapies (mostly tyrosine kinase inhibitors (TKI's)).
- Having complicated or unstable bone metastases (as judged by the clinician).
- Unstable heart disease, including unstable congestive heart failure, arrythmia, or myocardial infarction diagnosed within the last 3 months.
- Other malignancies in the last 2 years (except for adequately treated basal cell, superficial or in situ cancer of the bladder or the cervix).
- Have musculoskeletal problems precluding them to be physically active.
- Not understanding and speaking Dutch.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Cancer-related fatigue (FACIT-F)
Zeitfenster: From enrollment until 4 weeks after the end of treatment
|
Cancer-related fatigue (CRF) will be measured using the FACIT-F and EMA.
The Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) is a 13-item questionnaire with each item answered on a 5-point rating scale, which has been validated and frequently used in cancer populations.
The questionnaire is based on a 7-day recall period.
Scores range between 0 and 52, where higher scores represent lower fatigue levels.
The minimum important difference for the FACIT-F is between 3 to 4 points.
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From enrollment until 4 weeks after the end of treatment
|
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Cancer-related fatigue (EMA)
Zeitfenster: From enrollment until 4 weeks after the end of treatment
|
Regarding EMA, patients will install the m-path application on their smartphone.
Patients will be asked to fill in 3 prompts per day for 15 (M1 and M2) or 8 (M3 and M4) consecutive days, answering questions about fatigue ("I feel fatigued right now" from 1 (not at all) to 7 (very)).
The 3 prompts will be sent at a random time within 3 blocks per day (between 8h and 10h, between 12h and 14h, and between 18h and 20h).
Prompts will be available for 30 minutes and a reminder will be sent after 15 minutes.
Daily symptom rating will be calculated by taking the average of the 3 prompts and will be used for further analyses.
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From enrollment until 4 weeks after the end of treatment
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Physical activity
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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Physical activity (PA) will be measured during one or two week(s) (depending on the treatment phase) using an Actigraph GT3X and Dynaport Movemonitor+, both validated accelerometers.
Following recommendations on wear location, participants will be asked to wear the devices at the waist (on the same belt) during daytime and switch the Actigraph GT3X to the non-dominant wrist during the night (to measure sleep duration).
Valid PA data is considered when a patient has at least 8 hours wear time during waking hours.
The average daily step count (based on Dynaport Movemonitor+) and minutes of MVPA (based on Actigraph GTX3) per day of all valid days are the PA outcomes.
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From enrollment until 4 weeks after the end of treatment
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Symptoms of Dyspnea
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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Symptoms of dyspnea occurring during daily life activities will be assessed through the Chronic Respiratory Disease Questionnaire Self-Administered Standardized (CRQ-SAS).
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From enrollment until 4 weeks after the end of treatment
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Quality of Life (general)
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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The European organization for the Research and Treatment of Cancer Questionnaire (EORTC QLQ-C30) is a clinically valid and useful tool for assessing quality of life in lung cancer patients.
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From enrollment until 4 weeks after the end of treatment
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Quality of Life (lung cancer specific)
Zeitfenster: From enrollment until 4 weeks after the end of treatment
|
The European organization for the Research and Treatment of Cancer Questionnaire - lung cancer module (EORTC QLQ-LC13) is a clinically valid and useful tool for assessing quality of life, specifically for lung cancer patients.
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From enrollment until 4 weeks after the end of treatment
|
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Symptoms of stress, anxiety and depression
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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The Depression Anxiety Stress Scales-21 (DASS-21) has been developed as a single screening tool to measure comorbid depression, anxiety, and stress disorders in healthy individuals and represent a psychometrically viable option for health systems and clinicians when assessing distress in cancer patients.
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From enrollment until 4 weeks after the end of treatment
|
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Sleep quality
Zeitfenster: From enrollment until 4 weeks after the end of treatment
|
The Pittsburgh Sleep Quality Index (PSQI) is a valid and reliable tool to assess sleep quality across diverse populations.
Total scores range from 0 - 20, with a score of 5 or more indicating a poor sleep quality.
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From enrollment until 4 weeks after the end of treatment
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Quadriceps strength
Zeitfenster: From enrollment until 4 weeks after treatment
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A hand-held dynamometer (Microfet, Biometrics, NL) will be used to assess right isometric quadriceps strength.
Patients will be tested while sitting in an upright position.
The make test, as described by the ERS/ATS guidelines, will be performed.
The best of at least three reproducible measurements (<10% variability) will be used for analyses.
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From enrollment until 4 weeks after treatment
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Functional exercise capacity
Zeitfenster: From enrollment until 4 weeks after treatment
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Functional exercise capacity will be measured by a 1-min sit-to-stand (1MSTS) test and is a reliable and valid test for measuring functional exercise capacity in COPD patients.
Each participant will perform the test twice, with the highest value used for subsequent analyses.
Before and after the test, dyspnoea and fatigue will be monitored using the BORG-scale.
The heart rate and SpO2 will be monitored continuously throughout the test.
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From enrollment until 4 weeks after treatment
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Frailty
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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Frailty will be assessed according to the criteria of Fried et al.
The frailty phenotype is identified by the presence of three or more of the following components.
Unintentional weight loss, exhaustion, low activity, slowness and weakness.
Cut-off values for slowness and weakness were defined according to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) recommendations.
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From enrollment until 4 weeks after the end of treatment
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Volume of physical activity
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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Patients will be asked to wear a wearable (Garmin Vivosmart 5) throughout the whole study period as a measure of total volume of PA.
Whereas wearables will not provide a valid outcome to be used as primary outcome, the data are valid to provide an overall measure of physical activity.
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From enrollment until 4 weeks after the end of treatment
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Digital Mobility Outcomes (DMOs)
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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The DMOs, more specifically, gait pace, gait rhythm and gait bout-to-bout variability will be measured using the Dynaport Movemonitor +.
This outcome measure is part of the PA measurement and therefore requires no additional measurement.
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From enrollment until 4 weeks after the end of treatment
|
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Sleep time
Zeitfenster: From enrollment until 4 weeks after the end of treatment
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Sleep time will be measured using the Actigraph GT3X, worn on the non-dominant wrist during the night.
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From enrollment until 4 weeks after the end of treatment
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Occurence of (re)hospitalization, all-cause mortality and cancer-related mortality
Zeitfenster: From enrollment until 1 year after the start of the study
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The occurrence of (re)hospitalization, all-cause mortality and cancer-related mortality in the year after the start of the study will be reported.
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From enrollment until 1 year after the start of the study
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
14. September 2026
Primärer Abschluss (Geschätzt)
1. August 2028
Studienabschluss (Geschätzt)
1. Oktober 2028
Studienanmeldedaten
Zuerst eingereicht
24. August 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
28. August 2026
Zuerst gepostet (Tatsächlich)
2. September 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
17. September 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
16. September 2026
Zuletzt verifiziert
1. September 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Pathologische Prozesse
- Neubildungen nach Standort
- Neubildungen
- Erkrankungen der Atemwege
- Lungenkrankheit
- Neubildungen der Atemwege
- Thoraxneoplasmen
- Neoplastische Prozesse
- Pathologische Zustände, Anzeichen und Symptome
- Verhalten
- Anzeichen und Symptome
- Lungentumoren
- Ermüdung
- Neoplasma Metastasierung
- Motorik
Andere Studien-ID-Nummern
- ONZ-2026-0190
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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