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Project SHARE (Senior Health and Alcohol Risk Education)

Costs of Preventing Alcohol Problems in Older Adults

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00107640
Enrollment
1186
Registered
2005-04-07
Start date
2005-05-31
Completion date
2009-09-30
Last updated
2012-08-14

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

Conditions

Alcohol Consumption

Keywords

At-risk drinking, Alcohol education, Effectiveness, Cost-effectiveness

Brief summary

Older adults become more sensitive to alcohol, and alcohol also interacts adversely with their common medical conditions and medications. The aim of Project SHARE (Senior Health and Alcohol Risk Education) is to see whether patient and provider education can decrease risky alcohol use and reduce health care costs in persons 60 years of age and older.

Detailed description

Alcohol use in the elderly is an increasingly important public health problem. Alcohol-related risks and problems in older persons may come from the interaction between alcohol and diminished health or medication use. The proposed study is a randomized trial of the effectiveness and cost-effectiveness of an integrated patient-provider intervention to prevent risky alcohol use among older adults. The intervention will include a tested screening and education system that was developed especially for older adults and their providers, supplemented by a well-established intervention for physicians. The proposed research design involves randomization of 31 primary care physicians in seven clinics and their eligible patients aged 60+ to the intervention versus usual care.

Interventions

BEHAVIORALPatient-provider education

Experimental patients received an intervention consisting of the following components: written reports and educational materials, a telephone health educator intervention (at baseline, 3 and 6 months), and a brief provider intervention.

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH
University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 60 and over * At-risk drinkers * Patient of participating physician

Exclusion criteria

* Severe cognitive impairment * Terminally ill or deceased * Expected to move out of area or into nursing home within following year * Could not fill out written surveys in English * Likely dependent drinker

Design outcomes

Primary

MeasureTime frameDescription
At-risk drinking at 6 month followup6 monthsAt-risk drinking is alcohol use that (either alone or in conjunction with selected comorbidities, symptoms and/or medications) poses health risks. It is measured using the CARET instrument developed by Moore and colleagues.
At-risk drinking at 12 month followup12 monthsAt-risk drinking is alcohol use that (either alone or in conjunction with selected comorbidities, symptoms and/or medications) poses health risks. It is measured using the CARET instrument developed by Moore and colleagues.

Secondary

MeasureTime frameDescription
Mental Composite Score at 6 months6 monthsWe used self-reported SF12 data from baseline, 6- and 12-month written surveys to construct Mental Composite Score (MCS) and Physical Composite Score (PCS).
Healthcare utilization12 months (cumulative)We used self-reported data from 3-month, 6-month and 12-month written patient surveys to measure cumulative healthcare utilization by type (e.g., hospitalizations, emergency department visits, physician visits, etc.) over the twelve months following baseline.
Outpatient service costs12 months (cumulative)We used administrative data on clinic-based services linked to Medicare fee schedules to construct cumulative measures of outpatient service costs (from the Medicare perspective) for the twelve months following baseline.
Direct recruitment and intervention costs12 months (cumulative)We collected data on the resources used directly for recruitment (e.g., clinic-based staff time, phones, postage, etc.) and the intervention (e.g., cost of health educator time, supplies, opportunity costs of the physician's time, etc.) spent on the intervention, to construct overall measures of the per-patient cost of recruitment and intervention.
Health-related quality of life at 6 months6 monthsHealth-related quality of life (HRQL) is measured using the SF-6D.
Mental Composite Score at 12 month followup12 monthsWe used self-reported SF12 data from baseline, 6- and 12-month written surveys to construct Mental Composite Score (MCS) and Physical Composite Score (PCS).
Physical Composite Score at 6 month followup6 monthsWe used self-reported SF12 data from baseline, 6- and 12-month written surveys to construct Mental Composite Score (MCS) and Physical Composite Score (PCS).
Physical Composite Score at 12 month followup12 monthsWe used self-reported SF12 data from baseline, 6- and 12-month written surveys to construct Mental Composite Score (MCS) and Physical Composite Score (PCS).
Health-related quality of life at 12 month followup12 monthsHealth-related quality of life (HRQL) is measured using the SF-6D.
Depressive symptoms12 monthsDepressive symptoms are measured using the Geriatric Depression Scale.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026