Comparing Web, Group, and Telehealth Formats of a Military Parenting Program
NCT ID: NCT02973906
Last Updated: 2021-05-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
244 participants
INTERVENTIONAL
2014-06-01
2020-08-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparison of Couple-Based PTSD Treatment and Couple-Based PTSD Education
NCT01022203
Telehealth-Education-Based Program for Military Caregivers of Injured Service Members With Head Injuries
NCT02215187
Intensive Multi-Couple Therapy for PTSD Versus Relationship Education in Military Couples
NCT06047691
Mind-Body Skills Groups for the Treatment of War Zone Stress in Military and Veteran Populations
NCT01093053
Connecting Women to Care: Home-based Psychotherapy for Women With MST Living in Rural Areas
NCT03429166
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Combat deployment and related challenges are family stressors, associated with more negative parent-child interactions, ineffective and coercive parenting practices and lower levels of parenting satisfaction. Disrupted parenting practices are well-known predictors of risk for child adjustment difficulties that are precursors to youth substance use, including behavior problems, school failure, deviant peer association, and depression . These child adjustment problems can contribute to continuing parental stress, increasing parental distress, and further disrupting parenting.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
ADAPT Self Directed web
ADAPT Self Directed Web. In the self-directed web-only ADAPT condition, participants have access to the full ADAPT website (10 modules, online discussion forum)
ADAPT Self Directed web
In the self-directed web-only ADAPT condition, participants have access to the full ADAPT website (10 modules, online discussion forum
ADAPT individualized web-facilitated
This condition comprises access to the full ADAPT web program with augmentation of individual facilitator web support (i.e. the facilitator connects via Google Hangout). Facilitators meet with families at a mutually convenient time weekly (10-14 weeks, approximately 3 sessions per month).
ADAPT individualized web-facilitated
This condition comprises access to the full ADAPT web program as described above, with augmentation of individual facilitator web support (i.e. the facilitator connects via Google Hangout). Facilitators meet with families at a mutually convenient time weekly (10-14 weeks, approximately 3 sessions per month).
Group-based ADAPT
Groups will meet weekly for 120 minutes, at a time convenient to participants (usually early evening). Groups cover core ADAPT/PMTO topics
Group-based ADAPT
Groups will meet weekly for 120 minutes, at a time convenient to participants (usually early evening). Groups cover core ADAPT/PMTO topics:
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
ADAPT Self Directed web
In the self-directed web-only ADAPT condition, participants have access to the full ADAPT website (10 modules, online discussion forum
ADAPT individualized web-facilitated
This condition comprises access to the full ADAPT web program as described above, with augmentation of individual facilitator web support (i.e. the facilitator connects via Google Hangout). Facilitators meet with families at a mutually convenient time weekly (10-14 weeks, approximately 3 sessions per month).
Group-based ADAPT
Groups will meet weekly for 120 minutes, at a time convenient to participants (usually early evening). Groups cover core ADAPT/PMTO topics:
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* at least one child ages 5-12 in their custody and living with parent(s) in the home
* high speed internet access at home We will include both single-and two-parent families, as well as families where care is shared between non-partnered adults (e.g. grandparent and mother)
Exclusion Criteria
* an open child protection case for abuse or neglect in the family
* a serious child mental health diagnosis
* families who piloted material or participated in or are currently participating in the original ADAPT RCT.
18 Years
100 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Minnesota
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Abigail Gweitrz, PhD
Role: PRINCIPAL_INVESTIGATOR
Institute for Translational Research in Children's Mental Health University of Minnesota
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Institute for Translational Research in Children's Mental Health
Minneapolis, Minnesota, United States
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1407S52001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.