Somatic symptom and related disorders
Conditions
Interventions
None listed
Sponsors
Keio University School of Medicine Department of Neuropsychiatry
Keio University Faculty of Letters
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: <Healthy group> (1) Those who are able to participate in all experiments and answer the questionnaires. (2) Those who have no history of mental illness in the past, or those who have had a history of mental illness and have recovered for at least two years. (3) Those who have physical illnesses that the principal investigator judges will not interfere with their participation in the study. (4) Those who are at least 20 years old but less than 60 years old at the time of study participation. (5) Those who can provide written consent to participate in the study. <Disease group> (1) Those who can participate in all experiments and answer the questionnaire. (2) Those who have been diagnosed as somatic symptom and related disorders (including pain disorders, psychophysiological disorders, and autonomic disorders) by medical examination. (3) Those who have no history of psychiatric disorders other than somatic symptoms and related disorders, or those whose participation in the study is judged by the principal investigator to be safe even if they do have a history of psychiatric disorders. (4) Those who have physical illnesses that the principal investigator can judge will not interfere with their participation in the research. (5) Those who are at least 20 years old and under 60 years old at the time of participation in the study. (6) Those who can provide written consent to participate in the study.
Exclusion criteria
Exclusion criteria: (1) Patients who are judged by the principal investigator to have a serious mental illness that makes it difficult for them to participate in the research. (2) Patients who are judged by the principal investigator to have a serious physical illness that makes it difficult for them to participate in the research. (3) Patients who are judged by the principal investigator to have serious physical illnesses that make it difficult for them to participate in the research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Interrelationships among autonomic responses, interoception, and cognitive function | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)Autonomic responses (baroreceptor sensitivity, heart rate variability), 2) accuracy of interoception, 3) body image in the embody task, 4) meaningful decision traits (jumping to conclusion task, automatic thinking task), 5) sensory classification tasks, 6) pain threshold (using pain quantitative analyzer), 7)physical symptom assessment using variable questionnaires(PHQ-15, SSS-8, SSD-12, SSAS, SHAI, BPI, HADS, K10, PCS, MAIA, FFMQ, CFQ, AAQ2, SF-8, EQ-5D, TAS-20, AQ-J, IAS-J, IATS-J), 8) head MRI including resting state-functional MRI | — |
Countries
Japan
Contacts
Public ContactYuki Mashima
Keio University School of Medicine Department of Neuropsychiatry
Outcome results
None listed