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Testing ways to make patients' experience more comfortable after chest surgery

Measures to improve the experience of patients undergoing thoracic surgery: randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9g3xrqk
Enrollment
Unknown
Registered
2025-01-02
Start date
2025-01-10
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Lung Neoplasms

Interventions

Randomized Two-Arm Clinical Trial. Intervention group: 59 patients undergoing preoperative thoracic surgery will receive enhanced preoperative and postoperative education and access to follow-up educa
I02.233.332.500

Sponsors

Universidade Federal de São Paulo
Lead Sponsor
Universidade Federal de São Paulo
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients aged 18 years or over; both genders; undergoing invasive thoracic procedures whether by thoracotomy, sternotomy or videothoracoscopy

Exclusion criteria

Exclusion criteria: Patients under 18 years of age; patients who do not sign the free and informed consent form

Design outcomes

Primary

MeasureTime frame
Impact of a preoperative education program on patient-reported outcome measures (PROMs), determined through a questionnaire administered pre- and postoperatively—

Secondary

MeasureTime frame
No secondary outcomes are expected—

Countries

Brazil

Contacts

Public ContactAndré Miotto

Universidade Federal de São Paulo

miotto@unifesp.br+55(11)914486014

Outcome results

None listed

Source: REBEC (via WHO ICTRP)