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

A

Affiliated Hospital of Yunnan University

Status

Completed

Conditions

Depression in Old Age

Treatments

Other: selective prevention
Other: targeted prevention
Other: Waiting treatment.
Other: universal prevention

Study type

Interventional

Funder types

Other

Identifiers

NCT06132061
2023221

Details and patient eligibility

About

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.

Enrollment

327 patients

Sex

All

Ages

60 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

327 participants in 4 patient groups

Intervention group for universal prevention
Experimental group
Description:
Level 1 intervention (universal prevention) group
Treatment:
Other: universal prevention
Intervention group for selective prevention
Experimental group
Description:
Level 2 intervention(selective prevention) group
Treatment:
Other: selective prevention
Intervention group for targeted prevention
Experimental group
Description:
Level 3 intervention(targeted prevention) group
Treatment:
Other: targeted prevention
Control group
Other group
Treatment:
Other: Waiting treatment.

Trial contacts and locations

1

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Central trial contact

Tan Tang, Ph.D.

Data sourced from clinicaltrials.gov

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