The New York State Psychiatric Institute
New York, 10032, United States
NCT Number: NCT02294318
This pilot study goal is to compare two different treatments to help HIV positive patients reduce their concurrent drinking and non-injection drug use.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
New York, 10032, United States
The goal of this study is to compare the effects of brief motivational interviewing with participation in HealthCall to brief motivational interviewing alone on non-injection drug and alcohol use. HealthCall involves 2-3 minutes of daily smartphone use to track drug use, drinking behaviors and other aspects of health, followed by personalized feedback in a graph after 30 and 60 days of using the smartphone.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Age 18 and older; 2. During the prior 30 days, > 4 days of non-injection of cocaine, methamphetamine or heroin, one of which is identified by the patient as his/her primary drug During prior 30 days, > 1 day of binge drinking (>4 drinks on one occasion); Completion of medically supervised detoxification if such detoxification is required; HIV Positive ; Able to give informed consent
Exclusion criteria
Patient is currently psychotic, suicidal, or homicidal. Patient has injected any drug in the last 6 months Patient has definite plans to leave the greater New York metropolitan area within the study period.
Patient has gross cognitive/psychomotor impairment as evidenced on the Halstead-Reitan Trails (A+B) Patient does not speak English or Spanish Patient has a hearing and/or vision impairment that precludes smartphone use.
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HealthCall is a technology-based enhancement to brief MI to improve behavior outcomes. It is introduced to patients by the study counselor at the end of the MI session.
Other names: MI+HealthCall
Motivational Interviewing is a client-centered counseling approach for eliciting behavior change.
Time frame: 60 days
This outcome was derived from a Timeline Follow Back (TLFB) completed at the end of the intervention (day 60).
Time frame: 60 days
This outcome was derived from a Timeline Follow Back (TLFB) completed at the end of the intervention (day 60).
Time frame: 60 days
This outcome was derived from a Timeline Follow Back (TLFB) completed at the end of the intervention (day 60).
Time frame: 60 days
This outcome was derived from a Timeline Follow Back (TLFB) completed at the end of the intervention (day 60).
Research Foundation for Mental Hygiene, Inc.
Other
HealthCall: Brief Intervention to Reduce Drug Use in HIV Primary Care
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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