An observational study in Caregiver Burden, Health Literacy and Chronic Disease, sponsored by University of Yalova. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-24.
Sponsored by University of Yalova · Observational
This study aims to investigate the relationship between caregiver burden and health literacy among primary caregivers of patients with chronic diseases presenting to the emergency department. The study will be conducted in the Emergency Department of Yalova Training and Research Hospital and will include at least 300 caregivers. Data will be collected using a sociodemographic questionnaire, the Turkish Health Literacy Scale-32 (THLS-32), and the Zarit Burden Interview (ZBI). The findings are expected to contribute to a better understanding of caregivers' needs and to clarify the role of health literacy in caregiver burden among those providing care for individuals with chronic illnesses.
This study is planned to investigate the relationship between caregiver burden and health literacy among primary caregivers of patients with chronic diseases presenting to the emergency department. The role of primary caregivers in the management of chronic illnesses is critical, and their ability to access, understand, evaluate, and apply health-related information (health literacy) may influence both the quality of care provided and the utilization of emergency healthcare services.
The study will be conducted with at least 300 primary caregivers of patients admitted to the Emergency Department of Yalova Training and Research Hospital. Data will be collected using a sociodemographic questionnaire, the Turkish Health Literacy Scale-32 (THLS-32), and the Zarit Burden Interview (ZBI). The findings are expected to contribute to the identification of caregiver needs and provide evidence for the development of healthcare policies aimed at improving caregiver support and promoting the more efficient use of emergency healthcare services.
500 studies on the registry are indexed under Caregiver Burden; 164 are open to participants now.
This study's planned enrollment of 350 is above the median of 100 across 80 observational studies indexed under Caregiver Burden.
Browse Caregiver Burden studies →University of Yalova is the lead sponsor of 61 studies on the registry; 22 are open to participants now.
Counted across the registry records on this site, refreshed daily.
The target population of this study comprises the primary caregivers of patients diagnosed with chronic diseases, such as hypertension, diabetes mellitus, chronic obstructive pulmonary disease (COPD), heart failure, cancer, and neurological disorders, who are admitted to the Emergency Department of Yalova Training and Research Hospital.
The patient having visited the Yalova Training and Research Hospital Emergency Department.
Being at least 18 years of age. Being cognitively capable of answering the data collection tools (scales/questionnaires).
Volunteering to participate in the study and providing .
Exclusion Criteria:
Refusal to participate in the research voluntarily. Not being the primary caregiver for the patient. Inability to communicate or complete the scales due to cognitive or language barriers.
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Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Caregiver Burden Level (Zarit Burden Interview)
This outcome measures the physical, psychological, social, and financial stress experienced by caregivers using a 22-item Likert-type scale. Scores range from 0 to 88, where higher scores indicate a higher level of perceived caregiver burden. The scale evaluates the impact of caregiving on the individual's life through social and emotional domains.
Time frame: At the time of the face-to-face interview (approximately 15-20 minutes).
No study locations are listed for this record.
Start is estimated for Jul 2026; primary completion for May 2027, 10 months later.
How these figures are worked out, and which studies are left out of them.
This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.
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University of Yalova