Impact of the Presurgical Visit of Nursing on the Well-being of the Surgical Patient.

NCT03512561 | Completed

• 1 other identifier: EST-VPI-2017
• Study Type: observational
• Target: 356
• Locations: 1 country
• Sites: 1

Brief Summary

.A surgical intervention involves the participant and his / her family in a very stressful situation with a biopsychosocial alteration of the participant, often presenting a lack of knowledge of the surgical process from admission to hospital discharge. Researchers (nursing) began to make prior visits to the surgical procedure to reduce anxiety and provide information about the surgical process. The importance of the presurgical nursing visit (PNV) is sought, how to achieve a better health education throughout the surgical process, improve communication between professionals through standardized records, contributing to an optimal approach to the participant, increasing well-being, health and the satisfaction of the participant

Conditions

Nurse's Role; Preoperative Care; Patient Satisfaction

Outcome Measures

Primary Outcomes (1)

• The participant is satisfied throughout the surgical process, in relation to information, health education and personalized attention to the presurgical nursing visit (PNV)

  Number of participants who are satisfied with the experience of the surgical procedure and if this is what is explained in the presurgical nursing visit, for the evaluation of the importance of the visit in the surgical process.

  3 months

Secondary Outcomes (3)

• The participant feels well-being due to the care received by the professionals throughout the surgical process.

  3 month

• The participant has preoperative and postoperative anxiety in more than three months, relating it to the information provided in the presurgical nursing visit.

  3 months

• The participant perceives better quality of presurgical and postoperative life in more than three months; in relation to the training given during the pre-surgical nursing visit.

  3 months

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

All the patients who are going to be operated

You may qualify if:

• Patients who have undergone the pre-surgical nursing visit (personalized).
• Patients over 18 years of age
• Live accompanied and / or with own resources of help.
• Having signed the informed consent.

You may not qualify if:

• Not having signed the informed consent.
• Not having done the questionnaires after pre-surgical nursing visit (STAI, EQ-5D-5L)
• For surgical complications that do not allow the telephone survey, or focal groups.

Sponsors & Collaborators

• Corporacion Parc Tauli: lead

Study Sites (1)

Corporació Sanitària Parc Taulí

Sabadell, Barcelona, 08208, Spain

Location

MeSH Terms

Conditions

Patient Satisfaction

Condition Hierarchy (Ancestors)

Treatment Adherence and Compliance; Health Behavior; Behavior

Study Officials

• Francesc Zamora-Carmona, Nurse

  Corporacion Parc Tauli

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Nursing

Study Record Dates

• First Submitted: March 8, 2018
• First Posted: April 30, 2018
• Study Start: February 1, 2018
• Primary Completion: September 10, 2019
• Study Completion: October 1, 2020
• Last Updated: July 28, 2021

Record last verified: 2021-07

Data Sharing

• IPD Sharing: Will not share

Locations

ES (1)