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ORE - 30 Seconds (Oncologists Recommend Exercise in 30 Secs)

A Randomized Controlled Trial to Evaluate the Impact of Oncologists 'Exercise Recommendation on the Exercise Levels in Lung Cancer Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05497544
Acronym
ORE
Enrollment
60
Registered
2022-08-11
Start date
2022-07-01
Completion date
2025-07-01
Last updated
2022-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Brief summary

The O.R.E. - 30 seconds (Oncologists Recommend Exercise in 30 secs) trial aims to test the impact of oncologist recommendations on physical activity level, in patients with lung cancer.

Detailed description

Lung malignancy still remains the leading cause of cancer incidence and mortality worldwide. Despite the improvement in terms of innovative treatments, lung cancer and related therapies continue to be associated with severe physical, psychological, and social side effects. In recent years, several studies have investigated the potential role of physical activity (PA) and exercise (EX) as supportive therapy following a lung cancer diagnosis. Several randomized controlled studies provided evidence that EX is safe for lung cancer patients and may enhance several physiologic and psychologic outcomes. During the preoperative period, EX has demonstrated to increase cardiorespiratory fitness (CRF), and muscular strength, to reduce postoperative complications and length of hospital stay. Following surgery and/or during medical treatments, EX has shown to have a potent modulator effect, able to increase the health-related fitness capacities (especially CRF, muscular strength, and body composition), manage some treatment side effects, such as cancer-related fatigue, sleep disorder and anxiety/depression symptoms. In lung cancer settings, health-related fitness capacities, especially CRF, muscular strength and body composition, are resulted to be prognostic factors. For example, Jones et al. prospectively found that each 50 meters improvement in six minutes walking test (for assessing CRF) was associated with a reduction of 13% in the risk of death in patients with metastatic non-small cell lung cancer. Moreover, some preliminary observational data suggest that higher postdiagnosis PA is associated with lower recurrence, and specific and all-cause mortality in breast, colon, and prostate cancers. American Cancer Society and the American College of Sports Medicine recommend that cancer patients should achieve at least 90 min of moderate-intensity aerobic physical activity each week, with strength and flexibility exercises at least two times per week. Though the EX benefits are remarkable, most lung cancer patients result insufficiently active. Physician counseling has a positive impact on physical activity levels in sedentary adults, and even in the oncological setting can be a crucial key to engaging or improving PA or EX. Lung cancer patients reported that they prefer to receive PA information primarily from oncologists, and this counseling seems effective in improving PA levels. A randomized controlled trial indicated that 30-second oncologist counseling has a modest effect on PA behavior in breast cancer patients. In particular, at five weeks post-consultation, patients that received EX recommendation reported 3.4 metabolic equivalents of the task (MET)-hour of total EX per week (approximately 30 minutes of moderate-intensity) more compared to the usual care group. To date, limited data support the favorable role of oncologist recommendation, with no research focusing on lung cancer settings. To bridge this gap, we propose the O.R.E. - 30 seconds (Oncologists Recommend Exercise in 30 secs) trial to test the impact of oncologist recommendation on physical activity level.

Interventions

A verbal exercise recommendation will be provided. This recommendation will be reported also in the hospital resignation letter.

BEHAVIORALExercise recommendation plus guidebook group

This group will receive the exercise (verbal and written) recommendation. Additionally, the oncologist hand the patient a guidebook about exercise, specifically designed for cancer patients.

Sponsors

Universita di Verona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Confirmed diagnosis of lung cancer (from 0 to 24 months since diagnosis; * Stage I-IV; * Age ≥ 18 years; * ECOG (performance status) ≤ 1; * Written informed consent signed.

Exclusion criteria

* Obvious significant physical or psychological disabilities (e.g., wheelchair, severe anxiety); * Not able to speak, read or write in Italian; * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Exercise levelChange from baseline to 4 weeksExercise level will be evaluated with Godin's Shepard Leisure Time Exercise Questionnaire (0-700)

Secondary

MeasureTime frameDescription
Sedentary behaviorChange from baseline to 4 weeksSedentary behavior will be evaluated with the sedentary Behavior Questionnaire (0-500)
Quality of lifeChange from baseline to 4 weeksQuality of life will be evaluated with the European Organization for Research and Treatment of Cancer Quality of Life Core Questionnaire (0-100)

Other

MeasureTime frameDescription
Exercise levelChange from baseline to 8 weeksExercise level will be evaluated with Godin's Shepard Leisure Time Exercise Questionnaire (0-700)
Overall survivalChange from baseline to12 monthsOverall survival will be assessed through death from any cause.
Quality of lifeChange from baseline to 8 weeksQuality of life will be evaluated with the European Organization for Research and Treatment of Cancer Quality of Life Core Questionnaire (0-100)
Sedentary behaviorChange from baseline to 8 weeksSedentary behavior will be evaluated with the sedentary Behavior Questionnaire (0-500)
Progression free survivalChange from baseline to 12 monthsProgression free survival will be assessed through tumor progression or death from any cause
Treatment-related side effectsChange from baseline to 12 monthsTreatment-related side effects will be assessed using the Common Terminology Criteria for Adverse Events

Countries

Italy

Contacts

Primary ContactAlice Avancini, Ph.D.
alice.avancini@univr.it3403624264

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 28, 2026