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Well-being Skills for Reentry

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Enrolling

Conditions

Formerly Incarcerated Adults

Treatments

Device: Healthy Minds Program
Behavioral: Wellbeing skills for reentry

Study type

Interventional

Funder types

Other

Identifiers

NCT06975657
2024-1269
Protocol Version 12/10/2025 (Other Identifier)
A483000 (Other Identifier)

Details and patient eligibility

About

The goal of this clinical trial is to learn if a mindfulness skills training program has mental health benefits for people returning to the community following incarceration. The main questions it aims to answer are:

  • Does mindfulness skills training improve symptoms of anxiety and depression?
  • Do participants find this mindfulness program to be acceptable and feasible to participate in?

Researchers will compare outcomes for participants in the mindfulness training program to those in a waitlist control group who will receive the mindfulness program after the end of the study.

Participants will:

  • Complete an initial intake visit, consisting of an interview and questionnaires
  • Randomly be assigned to a mindfulness group or a waitlist control group
  • Participate in weekly mindfulness classes for 6 weeks (mindfulness group only)
  • Complete a set of questionnaires after the conclusion of the mindfulness classes
  • Complete a set of questionnaires and an interview 2 months after the conclusion of the mindfulness classes

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 or older
  • Formerly incarcerated in a local jail, state or federal prison
  • Can read, speak and understand English
  • Able to provide informed consent

Exclusion criteria

  • Suicidal ideation with some intent to act or with a specific plan and intent
  • Active psychosis
  • Daily or nearly daily use (over the past 3 months) of the following substances: cocaine, amphetamines, inhalants, sedatives or sleeping pills, hallucinogens, or opioids

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Wellbeing skills training
Experimental group
Treatment:
Behavioral: Wellbeing skills for reentry
Device: Healthy Minds Program
Waitlist control
No Intervention group

Trial contacts and locations

1

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Central trial contact

Study Team

Data sourced from clinicaltrials.gov

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