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Improving Depression Care for Elders: Coordinating Center

This Was a Five-year Seven-site Trial to Study the Cost-effectiveness of a Population Based Disease Management Program for Late Life Depression in Primary Care.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01561105
Acronym
IMPACT
Enrollment
1801
Registered
2012-03-22
Start date
1999-01-31
Completion date
2004-06-30
Last updated
2012-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depression, Dysthymic Disorder, Both Major Depression and Dysthymic Disorder

Brief summary

Purpose: To determine the effectiveness of the Improving Mood-Promoting Access to Collaborative Treatment(IMPACT) collaborative care management program for late-life depression.

Detailed description

This study tested an organized method of delivering care for late life depression in primary care. Specifically, the investigators evaluated the effectiveness of this intervention as compared to 'care as usual'. The investigators studied the effect of the intervention on clinical outcomes such as depressive symptoms, functional status, health related quality of life. They also determined the cost-effectiveness of the intervention compared to care as usual.

Interventions

OTHERIMPACT

IMPACT is a collaborative care management program for late-life depression

Sponsors

The John A. Hartford Foundation
CollaboratorOTHER
California HealthCare Foundation
CollaboratorOTHER
Hogg Foundation
CollaboratorUNKNOWN
Robert Wood Johnson Foundation
CollaboratorOTHER
University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum

Inclusion criteria

* Major depression or dysthymia as diagnosed by a structured diagnostic interview. * Patient plans to receive primary care at the study clinic for the next year.

Exclusion criteria

* Age under 60. * Current symptoms or history of psychosis or mania as determined by structured diagnostic interview. * Cognitive impairment as defined by a score less than 23 on a Mini Mental Status Examination. * Terminal illness - defined as having a life expectancy of less than 6 months. * Active alcohol abuse as determined by a screening interview. * High suicide risk as determined by current plan for suicide or a history of more than 3 prior suicide attempts in the past 10 years.

Design outcomes

Primary

MeasureTime frameDescription
Severity of depression symptomsSeverity measured by the 21-item Hopkins Symptom Checklist.

Secondary

MeasureTime frameDescription
Functioningmeasured by the Sheehan Health-Related Functioning Index

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026