The Effect of Informing Relatives of Patients With Short Messages

Kırklareli University

Status: Completed

Conditions: Short Message; Cardiovascular Surgery; Anxiety

Treatments: Other: SMS

Study type: Interventional

Funder types: Other

Identifiers

NCT05157789

KMarcinkowskiUMS

Details and patient eligibility

About

Surgical intervention is a planned or unplanned procedure performed to eliminate the existing or subsequent abnormal conditions in the individual's body, to reduce the effects of these conditions, or to remove the abnormal structures from the individual's body to eliminate the existing distress. While surgical interventions also cause anxiety in patients, it is known that they also cause significant anxiety in patients' relatives.This study was planned as a randomized controlled experimental study in order to examine the effect of this information on the anxiety level of the relatives of the patients by informing the relatives of the patients about the operation process with a short message during cardiovascular surgery.

In data collection; Introductory information form for the patient and patient relatives, a short message follow-up form, state and trait anxiety inventory will be used during the surgical intervention.

The sample of the study will be the relatives of the patients who are willing to participate in the study. Considering the change in the state anxiety scale scores between the experimental and control groups in the study of Baydemir S. (2019), it is calculated that there is a large effect size difference. Based on this finding, in order to test a large effect size (d=0.8) difference in anxiety scale scores of patient relatives between our experimental and control groups with 5% margin of error and 95% power, a total of 84 relatives of patients, 42 from each group, were included in the study. needed was calculated.

H0: Informing by text message has no effect on the anxiety of patient relatives.

H1: Informing by text message has an effect on the anxiety of patient relatives.

Enrollment: 84 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 18 years and over,
• To know Turkish,
• Being literate
• Having mental adequacy,
• Willingness to participate in the research,
• Having an active mobile line,
• Ability to use a telephone
• Being in the hospital before, during and after the operation

Exclusion criteria

• Be under the age of 18,
• Not knowing Turkish,
• Being illiterate
• Lack of mental adequacy,
• Lack of active mobile line,
• Inability to use the phone
• Absence from the hospital before, during and after the operation

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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84 participants in 2 patient groups

Sms group

Experimental group

Description:

Relatives of patients who were sent SMS

Treatment:

Other: SMS

Control Group

No Intervention group

Description:

Relatives of patients who were no intervation