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Recruiting NCT06893848

NCT06893848 Influence of the Culture Care Program on Patient Mobility After Thoracic or Abdominal Surgery: a Mixed-methods Study

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Clinical Trial Summary
NCT ID NCT06893848
Status Recruiting
Phase
Sponsor Haute Ecole ARC Sante
Condition Thoracic Surgery
Study Type INTERVENTIONAL
Enrollment 204 participants
Start Date 2025-03-10
Primary Completion 2026-05

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Culture Care program

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 204 participants in total. It began in 2025-03-10 with a primary completion date of 2026-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

A sedentary behavior in the postoperative phase has a negative impact on recovery from various types of surgery (e.g. abdominal, pulmonary, cardiac or esophageal). In fact, sedentary behavior in the days following surgery is associated with an increased risk of postoperative complications, longer hospital stays and, consequently, higher healthcare costs. Stimulating early mobilization and increasing the level of physical activity after surgery therefore remains a relevant current challenge. The Culture Care program will propose a new experience of the hospital towards an attractive and stimulating intrahospital environment, including art and culture. The hypothesis is that the innovative, positive hospital experience offered by the Culture Care program could contribute to increasing patients' mobility in the postoperative phase and thus reduce the sedentary behaviour compared with a control group included before the implementation of the program. The aim of this study is to explore the effect of the Culture Care program (Control group versus Culture Care group) on the mobility of patients hospitalized after thoracic or abdominal surgery, by determining the level of prediction in relation to the influencing covariates reported in the literature. The first quantitative part of this research project will compare the mobility of patients hospitalized after surgery, before (control group) and after the implementation of the Culture Care program (Culture Care group). Patients will be asked to wear an accelerometer for the first five post-operative days, and to complete three questionnaires (psychological well-being, physical recovery, perception of their mobility). Healthcare workers will be asked to complete a survey on their readiness to stimulate patients' mobility before and after the Culture Care program. The second part will be qualitative including individual semi-structured interviews with patients and healthcare workers during the Culture Care program, to gather their experiences.

Eligibility Criteria

Inclusion Criteria: * Admission to Surgical Units in the Surgical Department of the Hôpital de Neuchâtel implementing the Culture Care program. * Elective thoracic or abdominal surgery with an expected hospital stay of at least 2 days (i.e. discharge on postoperative day 3). * Neurocognitive and physical ability to complete questionnaires and individual participation in the Culture Care program. * Full capacity of discernment and signed informed consent to participate in the study. Exclusion Criteria: * Outpatient surgery. * Emergency surgery. * Mobility severely impaired prior to surgery: patients with 1 or 2 lower-limb amputations, patients with wheelchair mobility only, neurodegenerative diseases. * Bed restiction between POD 1 and POD 5 for medical reasons, i.e. surgery, post-operative complications or other pre-existing cardiorespiratory, neurological or orthopedic reasons. * Transfer to ICU * Only during the Culture Care phase, an unplanned transfer to another unit that does not have the Culture Care program (e.g. Medicine units). * Technical problem with the accelerometer (e.g. disfunctioning battery). * Allergic reaction to any dressing used to attach the accelerometer. * End-of-life patients.

Contact & Investigator

Central Contact

Jonathan Dugernier, PhD

✉ jonathan.dugernier@he-arc.ch

📞 0783057932

Frequently Asked Questions

Who can join the NCT06893848 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Thoracic Surgery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06893848 currently recruiting?

Yes, NCT06893848 is actively recruiting participants. Contact the research team at jonathan.dugernier@he-arc.ch for enrollment information.

Where is the NCT06893848 trial being conducted?

This trial is being conducted at Neuchâtel, Switzerland.

Who is sponsoring the NCT06893848 clinical trial?

NCT06893848 is sponsored by Haute Ecole ARC Sante. The trial plans to enroll 204 participants.

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