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Disease Management for Coronary Artery Patients

K

Kilis 7 Aralik University

Status

Completed

Conditions

Coronary Artery Disease
Patient Empowerment

Treatments

Other: Patient education

Study type

Interventional

Funder types

Other

Identifiers

NCT04556006
Kilis7AralikU

Details and patient eligibility

About

This randomized controlled trial was conducted with 58 patients hospitalized in the cardiology clinic of a state hospital. Personal Information Form, Anthropometric measurements, Framingham risk score, and compliance questionnaire (CQ) were used to collect the data.

Enrollment

58 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged 18 and over,
  • diagnosed with coronary artery disease for at least 2 months,
  • no hearing and vision problem,
  • no perception and expression deficiency,
  • not diagnosed with any psychiatric disease,
  • living in Kilis province,
  • voluntary to participate in the study.

Exclusion criteria

  • aged 18 under,
  • diagnosed without coronary artery disease for at least 2 months,
  • hearing and vision problem,
  • perception and expression deficiency,
  • diagnosed with any psychiatric disease,
  • no living in Kilis province,
  • no voluntary to participate in the study.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

58 participants in 2 patient groups

Control
No Intervention group
Description:
The patients in the control group received only the standard care provided by the clinicians. After the collection of post-test data, the content of the training was also explained to these patients and the study was completed by giving them the training guide.
Intervention
Active Comparator group
Description:
The training program was applied by the researcher who also work as an academic nurse. The contact information of the patients was obtained and the contact information of the researcher was also given to the patients. In order to consolidate the information given, the training guide was given to the patients in the intervention group. After the training, the patients in the intervention group were contacted again in the 2nd week by using face-to-face interview and in the 4th-8th and 12th weeks by phone calls. During these interviews, the questions of the patients, if any, were answered and the problems they faced regarding the disease management were tried to be solved. In the last interview, an appointment day was determined to meet face-to-face at home, workplaces or hospital according to the preferences of the patients.
Treatment:
Other: Patient education

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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