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Clinical Trials/NCT06132061
NCT06132061
Completed
Not Applicable

Research on Three-level Prevention and Intervention for Elderly Depression in Urban Community

Affiliated Hospital of Yunnan University1 site in 1 country327 target enrollmentJuly 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression in Old Age
Sponsor
Affiliated Hospital of Yunnan University
Enrollment
327
Locations
1
Primary Endpoint
Level of depression
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

The goal of this clinical trial is to compare the effect of three level interventions(universal prevention, selective prevention and targeted prevention) in elderly depression and find out the most efficient intervention path. The main questions it aims to answer are:

  • Whether the pre-disease three-level prevention model (universal prevention, selective prevention and targeted prevention) is applicable for elderly depression in urban communities;
  • Which level of intervention has the best effect on elderly depression.

Participants will be given the following treatments:

  • Level 1 intervention(universal prevention): Health education related to depression to strengthen the participants' self-care skills to reduce sub-health risk factors.
  • Level 2 intervention(selective prevention): Psychosocial interventions (including but not limited to cognitive behavioral therapy, acceptance commitment therapy, mindfulness training) aimed at risk factors to prevent more severe depressive symptoms.
  • Level 3 intervention(targeted prevention): Therapeutic psychosocial interventions (including but not limited to cognitive behavioral therapy, acceptance commitment therapy, mindfulness training) to reduce patients' depressive symptoms.

Researchers will compare control group to see if the three levels of intervention have a significant effect.

Registry
clinicaltrials.gov
Start Date
July 1, 2024
End Date
December 31, 2024
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Affiliated Hospital of Yunnan University
Responsible Party
Principal Investigator
Principal Investigator

Tan Tang

Lecturer, Department of Social Work

Affiliated Hospital of Yunnan University

Eligibility Criteria

Inclusion Criteria

  • Aged 60 and above;
  • Permanent residents of urban communities in China;
  • Geriatric Depression Scale (GDS-15) \< 9 points;
  • There are susceptibility factors such as living alone, poverty, and suffering from serious diseases.

Exclusion Criteria

  • There is suicidal behavior or risk;
  • A history of any other mental illness, including drug or alcohol dependence;
  • Those who have speech and hearing disorder and cannot communicate normally;
  • Geriatric Depression Scale (GDS-15) ≥10 points;
  • Do not agree to participate in the research.

Outcomes

Primary Outcomes

Level of depression

Time Frame: Measurements were taken at baseline, after intervention(3 months after baseline) and 6 months after intervention.The data will be reported through study completion, an average of 1 year.

A simplified version of Geriatric Depression Scale(GDS-15) will be used to mesure the level of depression. The scale has 15 items and asks the elderly to answer "yes" or "no" based on how they have felt in the past week. The "yes" is 1 point, "no" is 0 points. The higher the score indicates the more obvious depressive symptoms. The total score is 15 points. 0-4 points indicate no depression, 5-9 points indicate mild depression, and 10-15 points indicate moderate to severe depression.

Secondary Outcomes

  • Psychological flexibility(Measurements were taken at baseline, after intervention(3 months after baseline) and 6 months after intervention.The data will be reported through study completion, an average of 1 year.)

Study Sites (1)

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