Parenting Stress mHealth
a study on Mental Health Stress
Summary
- Eligibility
- for people ages 12 years and up (full criteria)
- Healthy Volunteers
- healthy people welcome
- Location
- at San Francisco, California
- Dates
- study startedcompletion around
- Principal Investigator
- by Johanna B Folk, PhD
Description
Summary
Parenting stress is a well-documented barrier to youth engagement in community-based substance use treatment. The current project aims to develop and evaluate a mobile health parenting stress intervention for caregivers of justice-involved youth, a population with high rates of substance use and low rates of treatment engagement.
Official Title
Reducing Parenting Stress to Facilitate Justice-Involved Youth's Treatment
Details
Justice-involved youth exhibit high rates of substance use and mental health symptoms, yet few receive treatment during detention or community re-entry. Once released into the community, caregivers must facilitate youth's treatment engagement, mobilizing significant resources and facing many barriers (e.g., transportation, mistrust) to do so. Parenting stress, which is heightened during youth detention and community reentry, is associated with greater perceived barriers to treatment, less youth therapeutic change throughout treatment, and premature treatment dropout. Addressing parenting stress improves youth treatment engagement and outcomes among youth exhibiting antisocial behavior, yet given the many barriers to treatment, novel approaches to intervention are needed; mobile health (mHealth) technology is one promising approach. Caregivers of justice-involved youth and system stakeholders are interested in mHealth treatment and mHealth addresses instrumental barriers (e.g., transportation) to treatment. Advances in technology and community engaged research allow for active stakeholder collaboration in mHealth application development, with no technological expertise required, through participatory informatics; caregiver involvement increases the likelihood the intervention will be relevant and efficacious. The purpose of this mixed-methods K23 study is to 1) develop a mHealth parenting stress intervention using participatory informatics; 2) assess the feasibility and acceptability of the participatory informatics approach and the intervention; 3) evaluate the intervention's preliminary efficacy in reducing parenting stress and increasing youth engagement in substance use or dual diagnosis treatment post-detention through a pilot randomized controlled trial; and 4) understand systems-level factors that could influence eventual system adoption and sustainability.
Keywords
Stress, parenting stress, juvenile justice, digital health, mHealth parenting stress app
Eligibility
You can join if…
Open to people ages 12 years and up
The following is a description for the inclusion criteria for aims 1 and 2 for caregivers participating in this research study.
Eligible caregivers must be the parent or legal guardian of a youth who is:
- currently detained in a juvenile detention center or correctional facility, mandated by the juvenile justice system to a congregate out-of-home placement (e.g., group home);
- 12-17 years old;
- has an identified substance use or substance use and co-occurring mental health need;
- and is scheduled to be released into the community to the care of the enrolled caregiver.
The following is a description for the inclusion criteria for aim 3 for system stakeholders participating in this research study.
Eligible behavioral health providers (e.g., substance use counselor) must:
- Provide substance use or dual diagnosis treatment justice-involved youth and their caregivers,
- be over 18 years old,
- and speak English fluently.
Eligible juvenile probation officers must be:
- 18 years or older
- and speak fluent English.
You CAN'T join if...
Exclusion criteria for all participants includes:
- lack of proficiency in English
- and cognitive impairment or active psychosis which precludes provision of informed consent.
Caregivers who do not have access to a device with internet access will also not be eligible as this would preclude them from being able to participate in the mHealth intervention.
Location
- UCSF Zuckerberg San Francisco General Hospital
accepting new patients
San Francisco California 94131 United States
Lead Scientist at UCSF
Details
- Status
- accepting new patients
- Start Date
- Completion Date
- (estimated)
- Sponsor
- University of California, San Francisco
- ID
- NCT05032742
- Study Type
- Interventional
- Participants
- Expecting 60 study participants
- Last Updated
Frequently Asked Questions
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study, which might include an external sponsor. Submitting your contact information does not obligate you to participate in research.
Thank you!
The study team should get back to you in a few business days.
You will also receive an email with next steps. Check your junk/spam folder if needed.
If you do not hear from the study team, please call 888-689-8273 and tell them you’re interested in study number NCT05032742.