Adaptive Goal-Directed Adherence Tracking and Enhancement
| Conditions | Phase | Intervention Type |
|---|---|---|
| Phase 2 |
|
Eligibility
- Ages Eligible for Study
- 21 years to 55 years
- Genders Eligible for Study
- Both
Keywords
Naltrexone, problem drinking, medication adherence, adherence, and smartphone
Sponsors
- NIH
- National Institute on Alcohol Abuse and Alcoholism (NIAAA)
- Industry
- Talaria, Inc
Inclusion Criteria
- problem or heavy drinkers
- age 21-55 years old
- located in the greater Albuquerque NM area
- interested in either reducing or stopping their drinking
- candidates for naltrexone pharmacotherapy
Exclusion Criteria
- participation in other naltrexone study
- unable to operate a smartphone
- significant psychiatric or physical illness
- current drug dependence
- current regular opioid use
- any recent nonmedical opioid use
- any lifetime opioid dependence
Detailed Description
Talaria, Inc., has designed an adherence tracking and enhancement system, called AGATE, which uses the text messaging and internet capabilities of modern cellular phones to address the problem of medication adherence in clinical care and clinical trial contexts. This trial will evaluate whether AGATE improves medication adherence in the context of a pharmacotherapy trial of naltrexone to treat problem drinking. All participants will be treatment-seeking problem drinkers who will receive naltrexone and medication monitoring over 8 weeks.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01349985
Overall Contact Backup
Locations
-
The Mind Research Network, University of New MexicoAlbuquerque, New Mexico United States()
Contact info
Christian Hendershot, Ph.D.505-504-1102chendershot@mrn.org