A Prospective Cohort Study on the Comorbid Depression in Patients With Newly-diagnosed Epilepsy

NCT04517058 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2021-12-28

No results posted yet for this study

Summary

Epilepsy is a chronic brain disease with recurrent seizures and the comorbidity of psychiatric diseases are very common. The prevalence of depression in patients with refractory epilepsy is about 60%. However, the early diagnosis is usually difficult due to the unclear mechanism and untypical clinical symptoms, and there are no extremely effective treatments for depression in patients with epilepsy until now. In this prospective, multi-center, cohort study, we aim to investigate and screen two different types of depression ("cognitive" and "somatic") in patients with epilepsy by using the combination of regular moods evaluating scales and heart rate variability instrument. The intervening methods of combining transcranial direct current stimulation (tDCS) and serotonin re-uptake inhibitors (SSRIs) are used to treat the patients with comorbidity of epilepsy and depression.

Conditions

Interventions

OTHER

psychology therapy

If the symptoms are mild, patients will get the psychology therapy. If it's necessary according to patients' willings, patients will be given SSRIs antidepressant therapy.

Sponsors & Collaborators

  • Huashan Hospital

    collaborator OTHER
  • Ruijin Hospital

    collaborator OTHER
  • Shanghai 10th People's Hospital

    collaborator OTHER
  • Shanghai 6th People's Hospital

    collaborator OTHER
  • Shanghai East Hospital

    collaborator OTHER
  • Shanghai Zhongshan Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-24
Primary Completion
2023-09-30
Completion
2023-12-31

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04517058 on ClinicalTrials.gov