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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05316207
Other study ID # TelenursingOHS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2020
Est. completion date April 21, 2021

Study information

Verified date March 2022
Source Hasan Kalyoncu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Introduction: Failure to follow-up patients by healthcare professionals after discharge may increase the development of anxiety and complications in patients. Aim: The aim of this study is to determine the effects of tele-nursing method to patients who have undergone Open Heart Surgery (OHS) after discharge on anxiety and some other complications. Material and Methods:This quasi-experimental randomized controlled study, which was conducted in a private hospital between November 2020 and April 2021, included 75 patients, 38 from the Intervention (IG) and 37 from the Control Group (KG). IG and CG patients were provided routine treatment and care. In addition to the IG, training and counselling were provided at least four times by phone calls between the first week after discharge and the end of the first month. Descriptive Form and State-Trait Anxiety Inventory (STAI-S and T) were administered to all patients before discharge, and STAI-S was administered at the end of the first month after discharge. Post-discharge complications were evaluated by medical doctor in both groups. These data, number of hospitalization and readmission rates were obtained from hospital records.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date April 21, 2021
Est. primary completion date April 21, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Eighteen years and older, - Able to speak and understand Turkish, - Without hearing, comprehension, vision and speech problems, - Open heart surgery for the first time, - Those who were not diagnosed with depression or anxiety disorder before surgery and didn't use medication for this purpose, - Having a mobile phone that can take photos by herself/himself or her/his attendants, - No serious complications to delay hospital discharge, - Patients who volunteered to participate were included in the study. Exclusion Criteria: Patients who wished to withdraw from the study after volunteering were excluded from the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Telenursing
From the end of the first week after discharge to the end of the first month, patients were counseled over the phone during the home process. Complications were followed up.

Locations

Country Name City State
Turkey Medical Park Hospital Gaziantep Sahinbey

Sponsors (1)

Lead Sponsor Collaborator
Hasan Kalyoncu University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Determination of change in anxiety levels between groups before discharge and one month after discharge Anxiety levels of all participants who met the inclusion criteria were measured using the state and trait anxiety scale in the pre-test. At the end of the first week after discharge, the intervention was started for the patients in the study group and the intervention was completed at the end of the first month after discharge. One month after discharge, the state anxiety levels were measured again with the state anxiety scale. State and trait anxiety levels were measured 72 hours before discharge for all participants who met the inclusion criteria.State anxiety levels of all participants were measured one month after discharge.
Secondary Rates of Complication Development The rate of total hospitalization before and after the intervention, the rate of admission to the hospital for examination, leg incision infection, effusion, chest incision infection and other complications that may occur within one month after discharge, according to the groups Complications developed in both groups were recorded at the end of the first week and the end of the fourth week after discharge.
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