← Back to all trials
Recruiting
NCT05708456
The Effect of Mobile Application on Hypothyroid Patients
Conditions: Hypothyroidism, Symptom Management, Symptoms and Signs, Mobile Application, Digital Health
Sex: All
Ages: 18 Years – 65 Years
Phase: NA
Enrollment: 80
Sponsor: Sakarya University
Location: Turkey
Summary
Hypothyroidism refers to the common pathological condition of thyroid hormone deficiency.
The annual incidence of hypothyroidism is 3.5 per 1000 in women and 0.6 in per 1000 men.
Hypothyroidism is seen 5-8 times more frequently in women than in men.
Patients with hypothyroidism have a higher prevalence of cardiovascular risk factors and often have metabolic syndrome features such as hypertension, increased waist circumference, and dyslipidemia.
Other signs and symptoms include bradycardia, slow speech, swelling in the eyes and face, weight gain, decreased sweating, hair loss, pallor, forgetfulness, decreased concentration, depression, irritability, tongue growth, loss of appetite, palpitations, decreased hearing, menstrual irregularities, muscle pains, and cramps.
Depending on all these signs and symptoms, hypothyroidism can negatively affect the quality of life of individuals.
Therefore, it is essential to reduce symptoms and to improve patients' abilities to manage them.
It is stated that the appropriate use of mobile health applications helps the patient to make informed decisions about health management and treatment.
Therefore, this study plans to investigate the effect of mobile technology on symptom management in individuals with hypothyroidism, whose symptoms range from mild to severe.
Eligibility Criteria
Inclusion Criteria:Able to communicate,Who agrees to participate in the study,Able to use a mobile phone with android or ıos (iPhone os) operating systemNo vision and dexterity problems,Without communication difficulties and cognitive impairment,LiterateBeing diagnosed with hypothyroidismExclusion Criteria:Pregnant patients,Those with a diagnosed psychiatric illness,Those who use antidepressants,Patients who experienced trauma or an acute illness during the study (12 weeks)
Source: ClinicalTrials.gov (NCT05708456). StuddyBuddy aggregates publicly available trial information.