ClinicalTrials.Veeva

Menu

Quality of Life in Chinese Working and School Age Population With MDD

S

Shanghai Mental Health Center

Status

Unknown

Conditions

Major Depressive Disorder
Remission

Treatments

Other: treatment as usual

Study type

Observational

Funder types

Other

Identifiers

NCT04986124
2020-76

Details and patient eligibility

About

Major depressive disorder (MDD) is a common mental illness with high prevalence and global burden. Previous studies revealed that over 70% patients in remission still had decreased quality of life, severe function impairment, low positive mental health score and poor coping ability. However, few studies focus on working and school age patients with MDD. A GBD survey showed that over 40% MDD patients are 15-50 years old. Therefore, we initiate the present multi-center cross-sectional survey to investigate the associations between clinical symptoms, cognitive function, occupational/study ability, and quality of life in Chinese working and school age population with MDD who are in remission.

Full description

This is a multi-center cross-sectional study. Patients with MDD who received medication treatment and achieved remission for at least 8 weeks will be enrolled. For all the participants, demographic information will be collected; clinical symptoms, cognitive function, occupational/study ability, and quality of life will be evaluated by using 17-items HAMD, PHQ-9, HAMA, PSQI, SHAPS, HCL-32, SDS, LEAPS, QOL-6, PFQ and THINC-it toolkit.

Enrollment

500 estimated patients

Sex

All

Ages

16 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Out-patients;
  • Men or women aged between 16 and 50, with junior high school education or above;
  • According to medical history, patients should be diagnosed with major depressive episode by two or above psychiatric doctors based on ICD-10 criteria;
  • According to assessment, patients should meet the DSM-5 criteria for MDD when in past episodes;
  • Patients received stable ant-depression medication treatment for at least 8 weeks before enrolment;
  • 17-item HAMD total score ≤ 7;
  • Willing to participate in this study, and sign an informed consent.

Exclusion criteria

  • HCL-32 total score < 12;
  • Diagnosed with bipolar disorder;
  • Suffering from some serious physical diseases (e.g. moderate or severe brain injury, central nervous system diseases, or other unstable physical condition affecting the whole body) adversely affects the performance on neuropsychological test or rating scales;
  • Received ECT in the past 6 months.

Trial design

500 participants in 1 patient group

MDD patients
Description:
No intervention.
Treatment:
Other: treatment as usual

Trial contacts and locations

1

Loading...

Central trial contact

Tao Yang, M.D.; Jun Chen, M.D., Ph.D

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems