MedSMA℞T Mobile ED
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: MedSMA℞T Mobile.
- Who it may be relevant to
- Registry conditions: Opiate-Related Disorders, Opiate Use Disorder, Opioid. Basic parameters: from 12 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Implementing MedSMA℞T Families in the Emergency Department Setting: A Game-based Approach for Improving Opioid Safety Among Adolescents and Parents
Overview
The goal of this clinical trial is to learn if a new smartphone-based intervention can help with factors related to opioid misuse in parents and adolescent/early adult children. The main question it aims to answer is: • Can this intervention improve knowledge of, and attitudes towards, opioid misuse over traditional opioid-related counseling alone? Participants will, in addition to receiving opioid counseling: * Join an online meeting with research staff to test the smartphone-based intervention * Report demographic information * Complete surveys about opioids * Complete a family medication safety plan * Complete surveys after 3, 6, and 9 months
Interventions
- Behavioral MedSMA℞T Mobile
MedSMA℞T Mobile is an innovative mobile digital health intervention that integrates technology-based learning to facilitate family communication and creation of a personalized Family Medication Safety Plan. The Family Medication Safety Plan (FMSP) is a tool for families to record important information about their medications and create a plan for safe use, storage, and disposal. Participants will play MedSMA℞T Mobile for up to 30 minutes at the first study visit.
Primary outcome measures
- Change in Adolescent Opioid Safety and Learning (AOSL) scale score over 9 month study [Time frame: Baseline, 3, 6, and 9 months.]
Secondary outcome measures (4)
- Change in Safe Opioid Storage Behaviour over 9 months [Time frame: Baseline, 3, 6, and 9 months.]
- Change in Opioid Disposal Behaviour over 9 months [Time frame: Baseline, 3, 6, and 9 months.]
- Change in Medication Understanding and Use Self-Efficacy (MUSE) scale scores over 9 months [Time frame: Baseline, 3, 6, and 9 months.]
- Change in Family Communication Behaviour Patterns over 9 months [Time frame: Baseline, 3, 6, and 9 months.]
Eligibility criteria
Inclusion criteria
- Adults who receive an opioid prescription from a study Emergency Department, AND
- who report having an adolescent, aged 12-18, living at home, AND
- who speak and understand English
- Each participant must have the ability to provide informed consent
Exclusion criteria
- Adults who do not receive an opioid prescription from a study Emergency Department AND/OR
- who do not have an adolescent, aged 12-18, living at home, AND/OR
- who do not speak or understand English
- Adults and/or adolescents who do not have the ability to provide informed consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Other
Study locations
United States · 3 centers
- Swedish American Hospital — Rockford
- East Madison Hospital — Madison
- University Hospital — Madison
Identifiers
NCT: NCT06848504 · 98853 · R18HS030202