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Clinical Feasibility of Disease Managing Mobile App for Hyperthyroidism

Clinical Feasibility of Disease-managing Mobile Application in the Patients With Hyperthyroidism

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05828732
Enrollment
100
Registered
2023-04-25
Start date
2022-03-01
Completion date
2023-12-31
Last updated
2023-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperthyroidism

Brief summary

This randomized controlled study aims to investigate the effects of using a mobile app that integrates with wearable devices to monitor heart rate, check self-reported symptoms, provide disease-related information, and set medication reminders for patients with thyrotoxicosis. The study intends to evaluate how the use of the app affects disease progression, quality of life, and health-related behaviors associated with the disease.

Interventions

OTHERUsing a mobile app that integrates with wearable devices

Using a mobile app that integrates with wearable devices to monitor heart rate, check self-reported symptoms, provide disease-related information, and set medication reminders for patients with thyrotoxicosis.

Sponsors

THYROSCOPE INC.
CollaboratorINDUSTRY
Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subjects who have been newly diagnosed or are currently undergoing treatment for thyrotoxicosis at Bundang Seoul National University Hospital. * Subjects must be able to use the smartphone app required for the use of wearable devices and their integration.

Exclusion criteria

* Subjects who have constraints on normal activity due to diseases other than thyroid dysfunction. * Subjects who are currently taking medication that affects heart rate. * Subjects with heart conditions such as arrhythmia that affect heart rate. * Subjects who cannot undergo antithyroid drug treatment and require surgery or radioactive iodine therapy.

Design outcomes

Primary

MeasureTime frameDescription
Scores of quality of life assessed by SF-36 surveybaseline (at enrollment)Scores of quality of life assessed by SF-36 survey
antithyroidal drug compliance6 weeks after baselineMedication adherence assessed by directly counting the remaining pills after taking the prescribed medication.
Knowledge about hyperthyroidism14 weeks after baselineA score measured through a test designed to assess the knowledge level about Graves' disease

Secondary

MeasureTime frameDescription
free T4baselineserum free T4 concentration
free T3baselineserum free T3 concentration
TSHbaselineserum free TSH concentration

Countries

South Korea

Contacts

Primary ContactJae Hoon Moon, MD
jaemoon76@gmail.com+82-31-787-7068

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026