Skip to content

An App to Reduce Cannabis Use Among Emerging Adults

Pilot Project 1. Feasibility Pilot of a JITAI to Reduce Cannabis Use Among Emerging Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05824754
Enrollment
122
Registered
2023-04-24
Start date
2024-02-21
Completion date
2024-05-28
Last updated
2025-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis Use

Keywords

Cannabis Use, Marijuana, Substance-Related Disorders, Mental Disorders

Brief summary

This study is being completed to pilot prevention methods to promote wellness and reduce risky behaviors, including the use of substances such as cannabis. This study will help researchers learn about ways of delivering this information that is both appealing and helpful to young adults who use mobile apps.

Interventions

OTHERJust-In-Time-Adaptive-Intervention (JITAI)

Behavioral: MiWaves behavioral messages Participants will be using the MiWaves mobile app for 30 days. When a participant is assigned to receive a message, a message will be randomly selected from a pool of intervention message sets. Messages are based in motivational interviewing and include affect management and behavioral economic strategies.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* Reside in the US * Speak and read English * Have a smartphone on which the app can be downloaded * Screen positive for cannabis use 3 or more times each week over the past month * Report motivation to change cannabis as 1 or higher (using scale of 0-10) * Meet Study verification criteria (i.e., use of CAPTCHA, IP address checks)

Exclusion criteria

* Use of Medical Cannabis * Failure to meet study verification criteria

Design outcomes

Primary

MeasureTime frameDescription
App Feasibility1 month% of participants who consented to the study who download the MiWaves app.
App Acceptability1 monthParticipants will complete acceptability ratings for the MiWaves app within their post-test assessment (percent with positive rating).

Countries

United States

Participant flow

Participants by arm

ArmCount
JITAI
Experimental: Within-participant micro-randomization Twice daily in the study, a participant is assigned to receive a message or no message. The micro-randomization will be performed by a reinforcement learning algorithm based on the participant's engagement with the intervention. Just-In-Time-Adaptive-Intervention (JITAI): Behavioral: MiWaves behavioral messages Participants will be using the MiWaves mobile app for 30 days. When a participant is assigned to receive a message, a message will be randomly selected from a pool of intervention message sets. Messages are based in motivational interviewing and include affect management and behavioral economic strategies.
122
Total122

Baseline characteristics

CharacteristicJITAI
Age, Categorical
<=18 years
7 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
115 Participants
Age, Continuous21.7 years
STANDARD_DEVIATION 2
Ethnicity (NIH/OMB)
Hispanic or Latino
19 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
103 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
6 Participants
Race (NIH/OMB)
Black or African American
12 Participants
Race (NIH/OMB)
More than one race
14 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants
Race (NIH/OMB)
White
89 Participants
Region of Enrollment
United States
122 participants
Sex: Female, Male
Female
65 Participants
Sex: Female, Male
Male
57 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 122
other
Total, other adverse events
0 / 122
serious
Total, serious adverse events
0 / 122

Outcome results

Primary

App Acceptability

Participants will complete acceptability ratings for the MiWaves app within their post-test assessment (percent with positive rating).

Time frame: 1 month

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
JITAIApp Acceptability90 Participants
Primary

App Feasibility

% of participants who consented to the study who download the MiWaves app.

Time frame: 1 month

Population: App feasibility outcome is operationalized as % of participants who consented to the study who download the MiWaves app. Not all that consented to the study were included in study flow since not all that consented downloaded the app. Therefore, the number analyzed for app feasibility is greater than the number in the participant flow.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
JITAIApp Feasibility122 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026