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Biosignals by Wearable Devices in Hypothyroidism

Clinical Application of Continuous Monitoring Data for Biosignals by Commercially Available Wearable Devices in the Patients With Hypothyroidism

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04332770
Acronym
Hypo_AT
Enrollment
45
Registered
2020-04-03
Start date
2019-06-14
Completion date
2020-10-15
Last updated
2021-01-05

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

Conditions

Hypothyroidism

Brief summary

This is a prospective observational cohort study. Monitoring continuous biosignals using wearable devices in thyroid cancer patients who are planned to withdraw their levothyroxine for radioactive iodine therapy. Through this, bio signals can be collected in the subjects in hypothyroid status. Physical activity, heart rate, and sleep data will be collected during the study period.

Detailed description

A prospective observational cohort study including two groups. Hypothyroid group: Patients with differentiated thyroid carcinoma underwent total thyroidectomy Patients who are planned to withdraw their levothyroxine for radioactive iodine therapy Biosignals will be monitored continuously using Fitbit devices Control group: Patients with differentiated thyroid carcinoma underwent total thyroidectomy Patients who are planned to get rhTSH (not to withdraw their levothyroxine) for radioactive iodine therapy Biosignals will be monitored continuously using Fitbit devices Thyroid hormone levels and continuously collected bio signals including activity, heart rate, and sleep data will be obtained during study period. Association between thyroid status and bio signals will be investigated.

Interventions

OTHERlevothyroxine withdrawal

All participants of this study are decided to get radioactive iodine therapy using levothyroxine withdrawal or human recombinant TSH injection prior to the study enrollment. That decision is independent with this study protocol. This study just collect continuous bio signals using wearable devices in the patients undergoing two different preparation methods for radioactive iodine therapy. That is why this study is an observational cohort study.

Sponsors

Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patients with differentiated thyroid carcinoma underwent total thyroidectomy * Patients who are planned to get radioactive iodine therapy * Patients who are able to use wearable device and smartphones

Exclusion criteria

* Patients who are not able to use wearable device and smartphones * Patients who are maintaining drugs affecting heart rate * Patients who have any other disease which can affect biosignals

Design outcomes

Primary

MeasureTime frameDescription
physical activity (steps)throughout the study period average 4 monthssteps data measured by wearable device, collected and recorded in 1 min increment
heart rate (beats)throughout the study period average 4 monthsheart rate data measured by wearable device, collected and recorded in 1 min increment
free T4 level (ng/dL)baseline (visit 1)thyroid hormone level
Zulewski hypothyroidism score ( point)baseline (visit 1)Scoring system to evaluate hypothyroid symptoms and signs
TSH level (mIU/L)baseline (visit 1)thyroid stimulating hormone level

Countries

South Korea

Outcome results

None listed

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