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Research and Engagement on Substance Use: Harnessing Awareness and Personalized Education (RESHAPE) to Improve Well-being and Self-efficacy

Research and Engagement on Substance Use: Harnessing Awareness and Personalized Education (RESHAPE) to Improve Well-being and Self-efficacy

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06952491
Acronym
RESHAPE
Enrollment
410
Registered
2025-05-01
Start date
2025-04-30
Completion date
2025-05-31
Last updated
2025-05-01

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

Conditions

Substance Use Disorder (SUD)

Keywords

Substance abuse

Brief summary

The goal of this study is to gather feedback on a potential program that collects and shares real-world information to help create products and services to support people who have substance use disorders.

Interventions

None listed

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Evidation Health
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* U.S. resident * Speaks, read, and understands English * Adults ≥ 21 years of age * Self-reported substance use disorder or at risk for substance use disorder as defined by cannabis use, tobacco use, illegal drug use, or prescription medication use for nonmedical reasons on at least 2-3 times in the past year * Self-reports at least one of the following health-related social needs as assessed by American Academy of Family Physicians Social Needs Screening Tool: * Housing instability * Non-reliable transportation * Food insecurity * Utility needs * Personal safety * Willingness and availability to participate in a recorded online interview (Phase 1A participants)

Exclusion criteria

* Participation in Phase 1A (among Phase 1B participants), to be assessed using participation history

Design outcomes

Primary

MeasureTime frameDescription
Willingness to participate in a future substance use disorder programBaselineNumber and percentage of interview and survey respondents reporting willingness to participate in a future substance use disorder program
Perceived usefulness and expected use of a future program's potential features and contentBaselineNumber and percentage of interview and survey respondents reporting that the future program's potential features are useful
To quantify and describe real-world health related social needs and/or substance use and/or demographics survey(s) previously collected on the Evidation platformFrom approximately 1 year prior to enrollment until study enrollmentNumber and percentage of interview and survey respondents who completed at least one health related social needs and/or substance use and/or demographics survey on the Evidation platform in the past year
Perceived expected use of potential features and content to be included in a program to improve well-being and self-efficacy for health promoting activitiesBaselineNumber and percentage of interview and survey respondents reporting that they expect to use each of the future program's potential features and content
To quantify and describe real-world data from a connected wearable device previously collected on the Evidation platformFrom approximately 1 year prior to enrollment until study enrollmentAverage number of days with valid steps, sleep, and heart rate data from a connected wearable device in the past year
To quantify and describe real-world data from responses to daily mood, stress, and sleep diaries previously collected on the Evidation platformFrom approximately 1 year prior to enrollment until study enrollmentAverage number of days with responses to daily mood, stress, and sleep diaries in the past year

Countries

United States

Outcome results

None listed

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