Tele Nursing Counseling on Anxiety and Patient Satisfaction in Same Day Surgery

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

160 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-01

Study Completion Date

2023-05-30

Brief Summary

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The study was planned to be conducted as a randomized controlled experimental study to examine the effect of preoperative tele-nursing counseling on anxiety and patient satisfaction in same day surgery.

The main Research Hypotheses are; Preoperative tele-nursing counseling has no effect on anxiety in same day surgery.

Preoperative tele-nursing counseling has an effect on anxiety in same day surgery.

Preoperative tele-nursing counseling has no effect on patient satisfaction in same day surgery.

Preoperative tele-nursing counseling has an effect on patient satisfaction in same day surgery.

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Detailed Description

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Power analysis was performed using the G\*Power (v3.1.7) program to determine the number of samples. The power of the study (α) was accepted as 0.05 (95% confidence level), Type 2 error probability (β) was accepted as 0.20 (80% power level) and the effect size of 0.46 in the relevant literature (Pehlivan, 2021) was taken into account, and the minimum required minimum in the groups was taken into account. It was found that taking the sample size as 74 would be sufficient. In the study, it was aimed to have a total of 148 participants, 74 for the control group and 74 for the experimental group. Considering the possible loss, the study was completed with a total of 160 patients, 80 of which were in the control group and 80 in the experimental group.

While evaluating the findings obtained in the study, SPSS (Statistical Package for the Social Sciences) version 25.0 (IBM Corp., Armonk, NY, USA) program will be used for statistical analysis.

Conditions

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Ambulatory Surgical Procedures

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The patients in the experimental group will be given a Preoperative Patient Information Brochure prepared by the researcher when they come to the hospital for the surgery date after the voluntary informed consent form is signed. Data were collected using the Introductory Information Form and the Surgery-Specific Anxiety Scale, and counseling was provided by tele-nursing information about the surgery process one day before the surgery. Patient's Perception of Nursing Care Scale was applied before leaving the hospital after day surgery.The patients in the control group were given a Preoperative Patient Information Brochure, which was prepared by the researcher on the day of the surgery, when they came to the hospital for the surgery date after signing the voluntary informed consent form. Data were collected using the Introductory Information Form and the Surgery-Specific Anxiety Scale. Patient's Perception of Nursing Care Scale was applied before leaving the hospital after day surgery.

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

The participant does not know which group he/she is in

Study Groups

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telephone counseling group

After signing the voluntary informed consent form, the patients in the experimental group were given a Preoperative Patient Information Brochure, prepared by the researcher when they came to the hospital for the surgery date. Data will be collected using the Introductory Information Form and the Surgery-Specific Anxiety Scale, and counseling was provided by tele-nursing information about the surgery process one day before the surgery.

Group Type EXPERIMENTAL

telephone counseiling

Intervention Type OTHER

One day before the operation, information was given about the operation process via tele-nursing and counseling was provided.

Control group

The patients in the control group were given a Preoperative Patient Information Brochure, which was prepared by the researcher on the day of the surgery, when they came to the hospital for the surgery date after signing the voluntary informed consent form.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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telephone counseiling

One day before the operation, information was given about the operation process via tele-nursing and counseling was provided.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Above 18 years old,
* Agreeing to participate in the research,
* Persons who will undergo day surgery in the field of general surgery, urology, orthopedic surgery, plastic surgery, neurosurgery,
* GKS score of 15,
* Not addicted to alcohol
* No psychiatric problems,
* Not using antipsychotic, antidepressant and anxiolytic drugs
* According to the ASA (American Society of Anesthesiologists) classification, ASA 1-2-3 -classification
* Speech and hearing impaired
* It is planned to include patients who have an open phone in the study.