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Active (not recruiting) Not applicable NCT07535671

The Effect of a Patient Education Program on Vitamin D Levels and Health Beliefs Regarding Vitamin D Use

No applicable phase (e.g. observational)
Conditions: Those Who Provided Written Informed Consent Female Gender Aged 18 Years and Older Hypothyroidism Disease Serum Vitamin d < 30 ng/dl

Sponsor: Karadeniz Technical University

trial.available_in: БГ
Overview
Background and Rationale: Vitamin D deficiency is a major public health concern. While clinical guidelines provide treatment protocols, medication adherence remains a significant barrier to achieving target serum levels. This study aims to evaluate whether a structured patient education program can improve health beliefs and adherence, ultimately leading to better clinical outcomes. Study Procedures: Participants identified with Vitamin D levels \<30 ng/mL will be randomized into two groups. Intervention Group: Patients will receive a face-to-face education session covering the importance of Vitamin D, correct usage, and potential side effects. They will also receive informative brochures and monthly follow-up phone calls to support adherence. Control Group: Patients will receive standard clinical care without additional structured education.Evaluation:Adherence will be monitored using the Medication Possession Ratio (MPR). Serum 25(OH)D levels and Vitamin D Health Belief Scale scores will be reassessed at the 6-month mark to compare the effectiveness of the intervention against the control group.
Who can participate
Inclusion Criteria: * Female, * Aged 18 years and older, * Hypothyroid disease, * Serum vitamin D level \< 30 ng/mL, * Providing written informed consent to participate in the study. Exclusion Criteria: * Male , * Under the age of 18, * Patients who do not provide written informed consent, * Serum vitamin D levels \> 30 ng/mL
Interventions
Educational with vitamin D
BEHAVIORAL
Locations 1
Turkey (1)
KTU Faculty of Medicine
Trabzon
Technical details
Status
Active (not recruiting)
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
01.11.2025
Completion date
01.06.2026
Registry ID
NCT07535671
Source
clinicaltrials.gov
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