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

I

Istanbul University - Cerrahpasa (IUC)

Status

Completed

Conditions

Ambulatory Surgical Procedures

Treatments

Other: telephone counseiling

Study type

Interventional

Funder types

Other

Identifiers

NCT05915624
IUCESEYHANAK001

Details and patient eligibility

About

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.

Full description

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.

Enrollment

160 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Exclusion criteria

  • Preoperative hospitalization
  • Patients undergoing emergency surgery
  • Patients who want to leave the study at any stage of the study

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

160 participants in 2 patient groups

telephone counseling group
Experimental group
Description:
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.
Treatment:
Other: telephone counseiling
Control group
No Intervention group
Description:
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.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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