The Turkish Validity-Reliability Study of the European Heart Failure Self-Care Behavior Scale-Caregivers Version
NCT ID: NCT05420688
Last Updated: 2024-01-22
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
150 participants
OBSERVATIONAL
2022-06-12
2023-09-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Validity and Reliability of the Turkish Version of the 4-Item Short Form of the Pain Anxiety Symptom Scale
NCT06758973
Determining the Effect of Home Care Training on Anxiety and Depression Levels of Caregivers
NCT07053553
Turkish of the Acupuncture Readiness Attitude Scale
NCT06807476
Turkish Validation of the Geriatric Pain Measure - Short Form
NCT06877481
Turkish Adaptation of Heart Health Self-efficacy and Self-Management Scale
NCT05939297
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
English Turkish translations will be made before starting the research. Afterwards, expert opinion will be taken for the suitability of the scale items. Then, the Turkish scale items will be translated back into English and the linguist's opinion will be taken that the scale can be applied. Language and content validity will be done for the scale form. The scale items will be translated into Turkish and expert opinions will be taken. Then, the Turkish scale items will be translated back into English and the linguist's opinion will be taken that the scale can be applied. Language validity and content validity will be done in the study. Explanatory Factor Analysis will be applied for the validity of the questionnaire. Kaiser Meyer Olkin(KMO) Test, which measures the adequacy of sample size as antecedent tests, and Bartlett's Test For Sphericity will be used to test sphericity. Factor Analysis Principal Component Analysis Method will be applied.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Heart Failure Group
This is a single-center, prospective, observational study. The assessment and reporting will be followed the Consensus-Based Standards for the Selection of Health Status Measurement Instruments (COSMIN) checklist.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* To be a caregiver for patients with heart failure for at least 1 year.
* Volunteer to participate in the research.
Exclusion Criteria
* be under the age of 18.
* Receiving hemodialysis treatment for less than 6 months.
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Harran University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
İbrahim Caner Di̇ki̇ci̇
Lecturer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
İbrahim C Di̇ki̇ci̇, MSc
Role: STUDY_DIRECTOR
Harran Üniversitesi
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Harran University
Sanliurfa, Türki̇ye, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
268347889
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.