Impact of the Presurgical Visit of Nursing on the Well-being of the Surgical Patient.
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| ClinicalTrials.gov Identifier: NCT03512561 |
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Recruitment Status :
Completed
First Posted : April 30, 2018
Last Update Posted : July 28, 2021
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| Condition or disease |
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| Nurse's Role Preoperative Care Patient Satisfaction |
In our Center, PNVs are carried out in the Ambulatory Area (External Consultations) in a specific and personalized nursing consultation, within an established and multidisciplinary program. One week before surgery, the patient and a family / primary caregiver are cited.
The PNV conducts a semi-structured interview; the content may vary according to the type of surgery, but in general it can be understood as all those nursing interventions; how to provide information, support, advice and training to the patient and his family (primary caregiver).
It is an innovative experience since it has been carried out for a short time. The PNV have been gradually restructured and continue to grow, since their establishment has been positively valued in the different services thanks to the experience gained and the numerous bibliographic references that demonstrate the beneficial results for the patient and the health system.
A total of 356 participants have been calculated (surveys answered in more than 3 months), taking into account an approximate population of 1,172 programmed interventions carried out in 1 year, with a confidence interval of 95%, accuracy of 3% a proportion of 5% and with an expected loss of 15%.
Sample:
Arthralplasia of knee / hip N 480 n 92 Cystectomies N 24 n 19 Esophagogastric with coloplasty N 24 n 19 Hysterectomy N 24 n 19 Colon / rectum N 192 n 65 Lumpectomy with sentinel lymph nodes N 222 n 74 Caesarean section N 206 n 68
| Study Type : | Observational |
| Actual Enrollment : | 356 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Impact of the Presurgical Visit of Nursing on the Well-being of the Patient Before a Surgical Process at the Parc Taulí Health Corporation. |
| Actual Study Start Date : | February 1, 2018 |
| Actual Primary Completion Date : | September 10, 2019 |
| Actual Study Completion Date : | October 1, 2020 |
- The participant is satisfied throughout the surgical process, in relation to information, health education and personalized attention to the presurgical nursing visit (PNV) [ Time Frame: 3 months ]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.
- The participant feels well-being due to the care received by the professionals throughout the surgical process. [ Time Frame: 3 month ]Number of participants who perceive welfare linked to the quality of care of the surgical process.
- The participant has preoperative and postoperative anxiety in more than three months, relating it to the information provided in the presurgical nursing visit. [ Time Frame: 3 months ]Number of participants who perceive pre and postsurgical anxiety and if it is linked to the information provided during the visit.
- 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. [ Time Frame: 3 months ]Number of participants who perceive an improvement in the quality of life and if it is linked to the information provided during the visit.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03512561
| Spain | |
| Corporació Sanitària Parc Taulí | |
| Sabadell, Barcelona, Spain, 08208 | |
| Principal Investigator: | Francesc Zamora-Carmona, Nurse | Corporacion Parc Tauli |
| Responsible Party: | Francisco Zamora Carmona, Nursing, Corporacion Parc Tauli |
| ClinicalTrials.gov Identifier: | NCT03512561 |
| Other Study ID Numbers: |
EST-VPI-2017 |
| First Posted: | April 30, 2018 Key Record Dates |
| Last Update Posted: | July 28, 2021 |
| Last Verified: | July 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

