Adrenocortical insufficiency, Adrenal insufficiency
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient Group: 1.Individuals with adrenocortical insufficiency undergoing hydrocortisone treatment exceeding 15mg per day 2.Individuals who possess a smartphone and are able to respond to questionnaires 3.Individuals able to wear a ring medical device and provide saliva samples 4.Individuals who have provided written informed consent Control Group: 1.Healthy individuals who possess a smartphone and are able to respond to questionnaires 2.Individuals able to wear a ring medical device and provide saliva samples 3.Individuals who have provided written informed consent
Exclusion criteria
Exclusion criteria: 1.Individuals who are unable to sleep while wearing a ring medical device 2.Individuals who are unable to utilize the study app 3.Individuals deemed inappropriate to participate in the study by physician judgement
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| An examination of cortisol levels in saliva and the correlation between physical activity data (such as depressive mood, sleep duration, body temperature, and pulse rates) gathered through the utilization of Ecological Momentary Assessment and IoT technology | — |
Secondary
| Measure | Time frame |
|---|---|
| The correlation between changes in physical activity readings on a daily basis and cortisol levels in saliva Assessment of the relevance of physical activity readings, cortisol levels in saliva, profile data, questionnaire responses, and medical records | — |
Countries
Japan
Contacts
Hokkaido University Hospital Diabetes and Endocrinology