Effect of Planned Visual Training on Heart Failure Patients
NCT ID: NCT06807671
Last Updated: 2025-02-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
110 participants
INTERVENTIONAL
2021-09-01
2022-03-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Control Group
No Intervention: Control group No intervention was made by the researcher during the study. Only data was collected. At the end of the study, visual training based on the planned Health Belief Model was given and all patients who continued the study were given brochures and heart-shaped key chains designed by the researchers.
No interventions assigned to this group
Experimental Group
Experimental: intervention group The sample of this simple-randomized controlled experimental study consisted of heart failure patients who applied to Manisa Celal Bayar University (MCBU) Hafsa Sultan Hospital Cardiology Polyclinic between September 2021 and March 2022. Patients who were determined by drawing lots according to their protocol numbers using the simple random sampling method were assigned to the intervention group. Patients assigned to the intervention group were given planned training based on the Health Belief Model. The intervention group was followed up for six months. A total of three interviews were conducted with the intervention group (First interview, 3rd month interview and 6th month interview).
Experimental Group
Patients in the intervention group received HBM based training for a period of 6 months. During the training, one-on-one interviews were provided with each patient. Patients were shown a power point presentation, a brochure, and 3 training videos. Any questions patients had were answered one-on-one.
Interventions
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Experimental Group
Patients in the intervention group received HBM based training for a period of 6 months. During the training, one-on-one interviews were provided with each patient. Patients were shown a power point presentation, a brochure, and 3 training videos. Any questions patients had were answered one-on-one.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Those with no communication problems,
* Those diagnosed with NYHA I-II heart failure,
* Those without cognitive impairment,
* Those who can understand and speak Turkish,
* Those who agree to participate in the study.
Exclusion Criteria
* Patients who want to leave the study,
* Patients with NYHA III-IV heart failure diagnosis,
* Patients diagnosed with cancer,
* Patients with diabetic foot or amputation.
18 Years
65 Years
ALL
No
Sponsors
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Celal Bayar University
OTHER
Responsible Party
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Dilan Deniz Akan
PhD
Locations
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Manisa Celal Bayar University
Manisa, Manisa, Turkey (Türkiye)
Countries
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Other Identifiers
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MCBU dilan deniz akan
Identifier Type: -
Identifier Source: org_study_id
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