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Anxiety and satisfaction of surgical patients

Anxiety and satisfaction of surgical patients undergoing educational intervention: randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9j7rs22
Enrollment
Unknown
Registered
2023-04-18
Start date
2023-05-02
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

Enhanced recovery after surgery

Interventions

Based on a previous study that evaluated the anxiety level of patients in the preoperative and postoperative period after an educational nursing intervention, the sample calculation was carried out as

Sponsors

Departamento de Enfermagem da Faculdade de Medicina de Botucatu
Lead Sponsor
Hospital das Clinicas da Faculdade de Medicina de Botucatu
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult patients undergoing elective colorectal surgeries in any segment; age equal to or greater than 18 years; both gender

Exclusion criteria

Exclusion criteria: Patients with any kind of difficulty in verbal and written communication or comprehension; patients submitted to surgical reoperation due to complications arising from a previous surgical procedure

Design outcomes

Primary

MeasureTime frame
Evaluate mediate preoperative anxiety score by applying the STAI anxiety assessment scale;Evaluate immediate preoperative anxiety score, through the application of the STAI anxiety assessment scale. The intervention group is expected to have less anxiety than the control group ;Assess the postoperative anxiety score by applying the STAI anxiety assessment scale. A greater score reduction between the pre and postoperative period is expected in the intervention group than in the control group;To measure patient satisfaction with the care provided in the late postoperative period, using the EORTC-32 scale. The intervention group is expected to have a higher satisfaction score than the control group

Secondary

MeasureTime frame
Evaluate postoperative pain, measured by applying the numerical verbal scale in the immediate and postoperative periods. It is expected that the intervention group will have a lower pain score than the control group;To measure the length of hospital stay, evaluated by the absolute number of length of hospital stay. It is expected that the intervention group will have a shorter hospital stay than the control group;Identify postoperative complications: hospital readmission, surgical re-approach, surgical site infection, intestinal obstruction, fistula, dehiscence, evaluated by the qualitative description in the hospitalization record. The intervention group is expected to have fewer postoperative complications than the control group

Countries

Brazil

Contacts

Public ContactCassiane Lemos

Universidade Estadual Paulista- Faculdade de Medicina de Botucatu

cassiane.lemos@unesp.br+55(14)3880-1293

Outcome results

None listed

Source: REBEC (via WHO ICTRP)