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Project SHARE (Senior Health and Alcohol Risk Education)

Phase 2
Completed
Conditions
Alcohol Consumption
Interventions
Behavioral: Patient-provider education
Registration Number
NCT00107640
Lead Sponsor
University of California, Los Angeles
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."

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1186
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Patient-provider educationPatient-provider educationExperimental 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.
Primary Outcome Measures
NameTimeMethod
At-risk drinking at 6 month followup6 months

At-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 months

At-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 Outcome Measures
NameTimeMethod
Physical Composite Score at 12 month followup12 months

We 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 months

Health-related quality of life (HRQL) is measured using the SF-6D.

Physical Composite Score at 6 month followup6 months

We used self-reported SF12 data from baseline, 6- and 12-month written surveys to construct Mental Composite Score (MCS) and Physical Composite Score (PCS).

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.

Mental Composite Score at 12 month followup12 months

We 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 6 months6 months

Health-related quality of life (HRQL) is measured using the SF-6D.

Depressive symptoms12 months

Depressive symptoms are measured using the Geriatric Depression Scale.

Mental Composite Score at 6 months6 months

We 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.

Trial Locations

Locations (1)

Sansum-Santa Barbara Medical Foundation Clinics

🇺🇸

Santa Barbara, California, United States

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