- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02400177
Parents Workgroup About Emotion Regulation
Parenting Workshop on Emotion Regulation
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The parents will answer questionnaires and Parent Development Interview (PDI) and the Five Minute Free Speech Sample (FMSS) as well as a number of other questionnaires.
Parents will be randomized between intervention group and control group. First session
- Introduction
- Setting expectations and goals
- General explanation of emotions and their development.
- How to recognize emotions? Why is it important to recognize them?
- Minding parents and child emotions. Second session
- Emotion Regulation (general explanation).
- Strategic for emotion regulation (Adults)
- Strategic for emotion regulation (children)
- Parental emotion regulation and the influence on the child emotion regulation
- Difficulties in ER among children with ASD Third session
- Three steps method: Feel, Think-Rethink, Regulate.
- Theory, explanation and implementation.
- Discussion: Role play of challenging highly affective parent-child interaction
Fourth session:
- Three steps method: Feel, Think-Rethink, Regulate.
- Theory, explanation and implementation.
- Discussion: Role play of challenging highly affective parent-child interaction The parents will do another PDI and will fill up the questionnaires
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Stanford, California, United States, 94306
- Stanford University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Parents of children with autism ages 3-18
Exclusion Criteria:
- If they cant understand English they can not be part of the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Emotion regulation training
This is a 4 sessions group workshop and 1 session individual pre-screening about parental emotion regulation and emotion co-regulation.
In this study the facilitators will give information about efficient strategies to regulate parent emotions and their children's emotions.
|
This is a workshop for parents that help them to understand how to deal with emotions generally and specifically with their ASD children's emotion
Other Names:
|
|
No Intervention: Control group
In this condition we will take all the measurement before and after the waiting list period. This group will go through the workshop after the measurements will be taken. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mentalization level
Time Frame: 1 month - 2 months
|
By the Parent Development Interview (PDI) before and after the workshop we measure the metallization level
|
1 month - 2 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Relationship coherence level
Time Frame: 1 month - 2 months
|
By the FMSS (5 min speech sample)
|
1 month - 2 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB32455
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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