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Acute Coronary Syndrome and Nurse Counselling

I

Iskenderun State Hospital

Status

Completed

Conditions

Coronary Artery Disease
Acute Myocardial Infarction

Treatments

Other: nursing counceling

Study type

Interventional

Funder types

Other

Identifiers

NCT06034054
DGulistan-01

Details and patient eligibility

About

The goal of this clinical trial is to examine in patients with acute coronary syndrome. The main questions it aims to answer are:

  • Does nurse counseling affect quality of life?
  • Does nurse counseling affect functional capacity?
  • Does nurse counseling affect knowledge, attitudes and beliefs about syndromes?

Participants will be trained using the training booklet, and nursing counseling will then be provided for six months.

If there is a comparison group: Researchers will compare with the control group to see if the nurse counseling has had an effect.

Full description

After obtaining verbal and written consent from the participants, they are required to answer the questions on the Diagnosis Form, Acute Coronary Syndrome Response Index, and Multiple Quality of Life Scale. Then, preliminary measurements will be made and a 6-minute corridor walking test will be applied. While the control group will be followed up routinely, the training booklet prepared for the intervention group will be explained orally. Participants will then be informed that they will be called monthly. They will be told that they can reach these monthly calls and consult the nurse when they need it. After this stage, interviews with patients will begin. The standard way of communication with the participants by the researchers is by telephone, and a total of 6 interviews will be provided, the first of which is in the 1st month after the application of the tests. In each call, all the information in the training booklet will be repeated, additional information will be given in line with the needs and demands of the person, their questions will be answered and the interview will be ended. Although it varies according to the individual interviewed, it is predicted that these telephone interviews will last for 30 minutes on average. Apart from these standard calls, individuals in need will be able to reach the researcher face-to-face during phone calls, text messages, instant messaging methods or hospital visits, and in this way, the counseling process will continue actively for 6 months. After six months, the final tests will be done.

Enrollment

66 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years old, diagnosed with Acute Coronary Syndrome and treated with a stent,
  • Treatment preventing communication is not a problem, literate,
  • There is no obstacle to performing the 6-minute walk test.
  • who did not accept to participate, were included in the study.

Exclusion criteria

  • <18 years of age,
  • Mental or cognitive impairment,
  • Diagnosed with SpO2 <80,
  • Peripheral arterial disease, lower extremity amputation, impaired tumor or open wound of lower extremity, and deep vein thrombosis, 6 munites corridor Walk test Parts of individuals who are contraindicated in making are not included.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

66 participants in 2 patient groups

Nursing counseling
Experimental group
Description:
The individuals included in nursing counseling group were given counseling by the research nurse for 6 months.
Treatment:
Other: nursing counceling
Control
No Intervention group
Description:
Individuals included in control group were followed up routinely in the outpatient clinic for 6 months.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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