A Web-based E-health Application for Active Illicit Opioid Users Providing Information About Overdose and Infection Risk Factors and Encouraging HCV/HIV Testing and Medication Assisted Treatment Seeking
| Registry | NCT03402672, acronym AWAITS |
|---|---|
| Status | Completed |
| Phase | Not applicable |
| Study type | Interventional; na, single group, masking: none, prevention |
| Enrollment | 24 (Actual) |
| Sponsor | University of Cincinnati (Other) |
| Conditions | Opioid-use Disorder, IV Drug Usage, Overdose, Drug Addiction, Substance Use Disorders |
| Interventions | self-administered, e-health application (Other) |
| Dates | start 2017-11-08, primary completion 2018-06-21, completion 2018-06-21, first posted 2018-01-18, last updated 2019-04-10 |
| Locations | 1 site in United States |
Related Papers Related Patents Related Grants Related Experts
AI Assistant Save
All trials for Opioid-use Disorder All trials for IV Drug Usage All trials of self-administered, e-health application
The purpose of this research study is to:
1. assess how participants like the AWAITS e-health application as measured by their feedback on the intervention
2. test the impact of AWAITS on knowledge about opioid overdose and risk-reduction strategies.
3. assess the proportion of participants who accept a list of local treatment providers
4. test the impact of AWAITS on interest in being tested for HCV/HIV.
The pre-post study of AWAITS will: 1) assess the acceptability of AWAITS as measured by participant feedback about the intervention; 2) test the impact of AWAITS on knowledge about opioid overdose, as measured by the OOTAS; 3) assess the proportion of participants who accept a list of local MAT treatment providers; and 4) test the impact of AWAITS on interest in being tested for HCV/HIV.
The acceptability of AWAITS will be assessed with a feedback form which includes questions about how helpful the intervention was (scale of 1-4), what the patient liked most and least about the intervention, and any suggestions for improving it. The average (and standard deviation) for the rated helpfulness of the intervention will be derived and the qualitative data about what they liked most and least about the intervention and suggestions for improvement will be tabulated. Pre-/post-changes in the percent of correct knowledge assessment items (i.e., about overdose and MAT) and interest in HCV/HIV testing will be analyzed using a Wilcoxon signed-rank test. The proportion of participants accepting a list of local MAT treatment providers will be calculated.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| AWAITS | Experimental | Other: self-administered, e-health application | Participants who meet criteria will receive the AWAITS self-administered, e-health application intervention. |
Sex: All, ages: 18 Years to any
Inclusion Criteria: 1. At least 18 years of age 2. Not enrolled in MAT per self-report 3. Self-reports illicit opioid use Exclusion Criteria: 3\. Does not acknowledge reviewing "Information Sheet for Research" within REDCap
| Facility | City | Country | Status |
|---|---|---|---|
| University of Cincinnati Addiction Sciences Division | Cincinnati, Ohio | United States |