PURPOSE: A Social Media Intervention for Parent Support
Parents United With Responsive Parents for Online Support and Education PURPOSE: A Social Media Intervention for Parent Support
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This study will take advantage of established peer training techniques to train parents of adolescents who are more experienced to help other parents better engage in services for their adolescent child. This pilot study marks the beginning of our long-term program of research focused on adapting intervention tools for delivery via e-technology platforms as a means for optimizing treatment effectiveness for youth. Thus, the proposed study will contribute to the scientific literature on the role of parental support in adolescent recovery as well as respond to NIDA's call for increased understanding of the feasibility and utility of social media as an option expanding the traditional treatment and face-to-face self-help groups. The proposed study has the following aims:
Aim 1: To develop PURPOSE, a social-media based intervention that provides information and coping tools for parents/guardians of adolescent children with a SUD. The theoretically grounded intervention will be peer-led, and will be developed and refined with feedback from experts, providers, parents, and adolescents.
Aim 2: To determine the feasibility and acceptability of PURPOSE that uses online peer-led intervention delivery. Trial testing will be conducted to iteratively refine content and procedures in order to optimize the engagement and usefulness of the intervention for parents.
Aim 3: To conduct a pilot control trial to provide preliminary data on this intervention so as to determine if social media-based parent support group involvement positively impacts parent outcomes (reduced stigma and distress, improved parent monitoring, and increased engagement in adolescent treatment) and adolescent outcomes (treatment retention and abstinence).
Studietyp
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
California
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Los Angeles, California, Förenta staterna, 90025
- UCLA Integrated Substance Abuse Programs
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Be the parent/guardian of an adolescent (under age 18) currently receiving out-patient treatment for SUD
- Have an active Facebook and email account
- Be able to read and write English
Exclusion Criteria:
- Any medical and/or psychiatric conditions which would require immediate or ongoing treatment that would make study participation difficult or harmful
- Already participating in an online support group for parents of teens in treatment
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: PURPOSE
Parents in the PURPOSE group will join a "secret" Facebook group for 2 months.
Groups will be lead by 2 peer leaders and include 20 parent participants.
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The first week of the intervention will focus on welcoming everyone to the facebook group and laying down the ground rules for participation. Each additional week of the intervention will focus on a specific topic to promote discussion and learning of each particular skill; however, questions and discussions on other relevant topics are always welcome and encouraged. Week 1: Welcome Week Week 2: SUD Basics Week 3: Problem of Stigma Week 4: Communication Skills Week 5: Parental Monitoring Week 6: Stress Management Week 7: Family and Valued Directions Week 8: Putting It All Together |
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Inget ingripande: Treatment as Usual (TAU)
Treatment as Usual parents will be contacted after 8 weeks to complete follow-up interview.
Will not receive PURPOSE intervention.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Adolescent Treatment History and Parental Engagement Questionnaire
Tidsram: 8 weeks
|
Parental report of child's treatment status, including enrollment date, primary reason for seeking treatment, and type of facility.
All parents will also report on number of informal parent/family support groups (e.g., AlAnon) and formal treatment sessions they have attended (baseline and follow-up).
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8 weeks
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Perceived Stigma of Addiction Scale
Tidsram: 8 weeks
|
The PSAS is an 8-item self-report questionnaire designed to assess perceptions of the prevalence of stigmatizing beliefs towards individuals with substance use diagnoses and treatment histories (baseline and follow-up)
|
8 weeks
|
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Parental Monitoring Questionnaire
Tidsram: 8 weeks
|
Relationship and disclosure constructs will be used from Stattin and Kerr's (2000) questionnaire of parental monitoring (baseline and follow-up)
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8 weeks
|
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Satisfaction and Usability Questionnaire
Tidsram: 8 weeks
|
Participants will report overall satisfaction and degree to which information provided was deemed applicable and helpful.
Likert-scale reports of satisfaction as well as responses to open-ended questions will be collected (PURPOSE intervention parents only and follow-up only).
|
8 weeks
|
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K-10 Scale of Psychological Distress
Tidsram: 8 weeks
|
The U.S. National Health Survey K-10 is a 10-item screening scale used to assess the degree of non-specific psychological distress over the past 30 days (baseline and follow-up)
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8 weeks
|
Samarbetspartners och utredare
Samarbetspartners
Utredare
- Huvudutredare: Marya Schulte, Ph.D., University of California, Los Angeles
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- R21DA039459 (U.S.S. NIH-anslag/kontrakt)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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