The Effect of Telephone Nursing Education and Counseling Services Given to Satisfaction Level and Self-Care Strength

NCT05487638 | Completed

• 1 other identifier: vesile2022
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

In the post-discharge period, it is important to follow the patients from home by telephone and to provide the necessary nursing education and counseling services, increasing the self-care powers of the patients, increasing their quality of life, adapting to the social life after discharge and facilitating the patient's adaptation to the post-discharge process. When the literature is examined, it can be said that the study is original since there are no studies on this subject. The aim of this study is to determine the effect of nursing education and counseling service given to patients who have undergone CABG, on the level of discharge satisfaction and self-care power of patients.

Conditions

Postoperative Complications

Keywords

surgical site infection; coronary artery bypass graft; constipation; sleep disorders; pain

Outcome Measures

Primary Outcomes (2)

• Discharge Training Satisfaction Scale star_border Discharge Training Satisfaction Scale

  Discharge Education Satisfaction Scale is in five-point Likert type (from 1 to 5): 3 items about discharge process, 3 items about personal information, 7 items about home care, 3 items about infection, 5 items about controls, It consists of 21 questions in total.

  up to 1 month

• Self-Care Strength Scale

  It was adapted into Turkish by Nakhchivan N. This scale consists of 43 descriptive statements. Each statement was scored from 0 to 4 in the 5-point Likert-type Self-Care Scale. Scoring of the scale items is (0) does not describe me at all, (1) does not describe me very well, (2) I have no idea, (3) describes me a little, (4) describes me a lot. It describes the self-care powers of patients.

  up to 1 month

Study Arms (2)

experimental Group

EXPERIMENTAL

Training was given to the patients once a week, starting on the second day after discharge, four times in total. Increasing the level of knowledge about infection control, wound care, post-CABG care, using drugs as prescribed, hygiene, excretion (things to be done to avoid constipation), nutrition (diet and diet compliance after CABG), bleeding control, proper sleep and rest positions, deep breathing and coughing exercises, maintaining a healthy weight, what to pay attention to while taking a bath, pain management and methods of coping with pain, relaxation techniques, walking and exercise, returning to social life, reducing anxiety and depression, using elastic stockings and chest corsets, controlling Training was given on the subjects of notifying the due dates, emotional adjustment and coping methods with symptoms. After 1 month of training, at the end of the 4th week, the patients were asked to fill out the Discharge Education Satisfaction Scale and the Self-Care Strength Scale.

Other: Nursing Education and Counseling Service Provided to Patients by Video Calling on the Phone

Control Group

NO INTERVENTION

On the other hand, no intervention was made in the control group and after discharge, the personal information form, the Discharge Training Satisfaction Scale and the Self-Care Strength Scale were filled. At the end of the 4th week, the patients were asked to fill out the Discharge Education Satisfaction Scale and the Self-Care Strength Scale.

Interventions

Nursing Education and Counseling Service Provided to Patients by Video Calling on the Phone OTHER

Nursing Education and Counseling Services were provided to the patients by video calling on the phone for the problems they may encounter in the postoperative period.

Also known as: İntervention Group

experimental Group

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patient between the ages of 18 and 75,
• literate, who could speak Turkish,
• who had undergone CABG surgery for the first time,
• who could be contacted,
• who did not have a mental illness,
• whose discharge was decided,
• who stayed in the hospital for at least 2 nights after the operation,
• who voluntarily agreed to participate in the study were included.

You may not qualify if:

• patients whose surgery was delayed
• Patients who refused to participate in the study
• developing mental problems
• patients whose discharge was canceled

Sponsors & Collaborators

• Ataturk University: lead

Study Sites (1)

Atatürk University

Erzurum, Palandöken, 25000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Postoperative Complications; Surgical Wound Infection; Constipation; Sleep Wake Disorders; Pain

Condition Hierarchy (Ancestors)

Pathologic Processes; Pathological Conditions, Signs and Symptoms; Wound Infection; Infections; Signs and Symptoms, Digestive; Signs and Symptoms; Nervous System Diseases; Neurologic Manifestations; Mental Disorders

Study Officials

• Vesile Eskici İlgin, Dr

  Ataturk University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: August 2, 2022
• First Posted: August 4, 2022
• Study Start: June 3, 2022
• Primary Completion: July 15, 2022
• Study Completion: August 1, 2022
• Last Updated: August 4, 2022

Record last verified: 2022-08

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)