Healthy Living as You Age

NCT ID: NCT00379093

Last Updated: 2009-07-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 631 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-08-31
• Study Completion Date: 2008-07-31

Brief Summary

Older persons who drink can be vulnerable to negative consequences of drinking. This trial aims to prevent harm from alcohol use in older adults through a program of screening and brief advice followed up with several health education phone calls.

Detailed Description

Approximately 50% of persons aged 65 years and older drink alcohol. Older persons are particularly susceptible to adverse consequences of drinking such as falls, depression, sleep disorders, stomach upset, hypertension, and alcohol/drug interactions. This is because of age-related changes in the body that affect how older persons react to alcohol and also because of the age-associated increases in illness and medication use.

In the current project we aim to see if screening and brief advice given to older risky drinkers in a physician's office followed by up to 3 health education phone calls may reduce their risks associated with alcohol use. We plan to use a newly developed and tested measure, the Comorbidity Alcohol Risk Evaluation Tool (CARET), to screen for older persons (aged 55 and older) whose use of alcohol alone or in combination with their illnesses, symptoms, and medication use may be causing them harm, or increasing their risk for harm. Persons whose responses on the CARET indicate they might be risky drinkers will be randomized to receive either a brief intervention to reduce their risks or usual care.

The intervention will have the following components:

A) At the time of the recruitment visit, all intervention group patients will receive:

1. A personalized risk report;

2. An educational booklet titled "Healthy Drinking as You Age";

3. A drinking diary;

4. Brief advice to reduce their drinking by their physicians;

B) After the recruitment visit, all intervention group patients will receive up to 3 telephone calls from a health educator. After each call, intervention group patients may choose to receive a letter updating their health risks. Also, at the conclusion of their interaction with the health educator, they may choose to have a letter summarizing the calls sent to their physician.

At the time of the recruitment visit, control group patients will receive a booklet on a variety of healthy behaviors titled "Healthy Living as You Age." Both control and intervention group patients will receive a telephone call from a research associate 3 months and 12 months after initial enrollment in the study to administer the CARET again.

We will analyze our results to look for differences between the intervention and control groups at 12 months in the a) proportions of them identified as risky drinkers by the CARET; b) the amount they drink; c) the numbers of risks identifying those persons who are still risky drinkers and d) the difference in their expectations regarding aging.

Conditions

Alcohol Related Disorders; Alcohol Drug Interactions

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: SINGLE

Interventions

Brief advice

The intervention will have the following components:

A) At the time of the recruitment visit, all intervention group patients will receive:

• A personalized risk report;
• An educational booklet titled "Healthy Drinking as You Age";
• A drinking diary;
• Brief advice to reduce their drinking by their physicians;

B) After the recruitment visit, all intervention group patients will receive up to 3 telephone calls from a health educator. After each call, intervention group patients may choose to receive a letter updating their health risks.

Also, at the conclusion of their interaction with the health educator, they may choose to have a letter summarizing the calls sent to their physician.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• At least 55 years of age
• Seeing a participating physician (internists or family physicians employed at any of the participating sites)
• Have had at least one alcoholic drink in the last week

Exclusion Criteria

• Too ill to participate
• Have received substance abuse services in past 3 months

• Minimum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

NIH

Sponsor Role: lead

Responsible Party

University of California, Los Angeles, David Geffen School of Medicine

Principal Investigators

Alison A. Moore, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

UCLA DOM-Geriatrics

Locations

UCLA Department of Medicine, Geriatrics Research Center

Los Angeles, California, United States

Countries

United States

Other Identifiers

NIH Grant 5 RO1 AA 013937

Identifier Type: -

Identifier Source: secondary_id

NIAAA-MOO-013937

Identifier Type: -

Identifier Source: org_study_id