Last reviewed · How we verify

NCT03090958: AQ

AllyQuest: Engaging HIV+ YMSM in Care Through Social Networking and Gamification

Completed NA Results posted Last updated 11 July 2018
What this trial tests

NA trial testing AllyQuest in Hiv in 20 participants. Completed in 3 January 2017.

Timeline
1 August 2015
Primary endpoint
3 January 2017
3 January 2017

Quick facts

Lead sponsorUniversity of North Carolina, Chapel Hill
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment20
Start date1 August 2015
Primary completion3 January 2017
Estimated completion3 January 2017

Drugs / interventions tested

Conditions studied

Sponsor

University of North Carolina, Chapel Hill

Who can join

Adults 16 to 24, male only, with Hiv or HIV/AIDS. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Number of Participants That Were Enrolled of Those Screened Primary · 4 weeks

Feasibility of AllyQuest will be based on recruitment success as measured by the total number of individuals who are screened vs. the total number of individuals who are recruited and subsequently enrolled.

GroupValue95% CI
AllyQuest Pilot20
Number of Participants That Missed Follow up Interviews Primary · 4 weeks

Feasibility of AllyQuest will be based retention as measured by the number of missed follow up interviews. Follow up attempts will be documented.

GroupValue95% CI
AllyQuest Pilot17
Average Number of Days Participants Logged in. Primary · 4 weeks

Feasibility of AllyQuest will be based on usage as measured by the average number days participants access the app.

GroupValue95% CI
AllyQuest Pilot21.2± 14.1
Number of Individuals Who Enroll But do Not Participate Primary · 4 weeks

Feasibility of AllyQuest will be based on the number of individuals who enroll and do not participate.

GroupValue95% CI
AllyQuest Pilot3
Average Total Time in Minutes Participants Spent Using App. Primary · 4 weeks

Feasibility of AllyQuest will be based on usage as measured by the average time spent using app.

GroupValue95% CI
AllyQuest Pilot158.4± 114.1
Average Number of App Actions by Participants Primary · 4 weeks

Feasibility of AllyQuest will be based on usage as measured by the average number of activities completed (daily quests), articles read, and social posts made.

Articles read
GroupValue95% CI
AllyQuest Pilot8.8± 7.3
Social wall posts
GroupValue95% CI
AllyQuest Pilot12.9± 12.5
Daily Quests
GroupValue95% CI
AllyQuest Pilot15.8± 13.5
Average Days Participants Logged Medications. Primary · 4 weeks

Feasibility of AllyQuest will be based on usage as measured by the average number of days participants logged their medications in the app.

GroupValue95% CI
AllyQuest Pilot19.4± 13.2
System Usability Scale Scores Secondary · 4 weeks

Acceptability of AllyQuest will be measured by the System Usability Scale (SUS). An 11-item, 7-point Likert scale of subjective assessments of usability (1=strongly agree; 7=strongly disagree). The SUS is technology independent and provides a global measure of system satisfaction and sub-scales of usability and learnability.

Would use this app frequently
GroupValue95% CI
AllyQuest Pilot4.41± 1.18
App was easy to use
GroupValue95% CI
AllyQuest Pilot4.76± 0.56
Felt very confident using the app
GroupValue95% CI
AllyQuest Pilot4.47± 1.01
App is accurate
GroupValue95% CI
AllyQuest Pilot4.53± 1.01
App is dependable
GroupValue95% CI
AllyQuest Pilot4.53± 0.62
Interaction with app is consistent
GroupValue95% CI
AllyQuest Pilot4.18± 0.95
Found app unnecessarily complex
GroupValue95% CI
AllyQuest Pilot1.65± 0.86
Would need technical assistance to use app
GroupValue95% CI
AllyQuest Pilot1.71± 1.16
Client Satisfaction Questionnaire Score Secondary · 4 weeks

Acceptability of AllyQuest will be assessed using the Client Satisfaction Questionnaire (CSQ-8). The CSQ-8 was used to assess global intervention satisfaction. The CSQ-8 has eight items (quality of app, kind of service received from app, app met needs, recommend app to a friend, amount of help received from app, effectiveness of app for dealing with health problem, overall satisfaction, and willingness to use the app again). These domains are assessed on a 4-point response scale with individually specified anchors. Participant responses are scored from 1 to 4, and thus the possible total score

GroupValue95% CI
AllyQuest Pilot27.8± 5.9

Sponsor's own description

AllyQuest is a novel, high impact secondary prevention intervention delivered via mobile phones to improve linkage and engagement in care among newly diagnosed HIV+ young men who have sex with men (YMSM). The features of the intervention aim to target previously identified barriers to care among newly diagnosed youth, namely, low HIV health literacy, lack of social support, and internalized stigma related to their diagnosis. AllyQuest will be an interactive mobile phone intervention for HIV+ YMSM that utilizes social networking, game-based mechanics and a story-based framework to guide behavior change. Grounded in Social Cognitive Theory, narrative communication and the principles of persuasive technology, the intervention is designed to capitalize on social involvement as a means through which HIV+ YMSM can receive information and social support, experience social norms and reflective appraisals, and feel a sense of connectedness to peers.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Hiv

Currently open trials in the same condition.

Other University of North Carolina, Chapel Hill trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03090958.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing