Kidpower Camp - Structured Games or Playgroup
Primary Purpose
Anxiety Disorders
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Structured games
Playgroup
Sponsored by
About this trial
This is an interventional treatment trial for Anxiety Disorders focused on measuring Effortful Control, Preschool, Error-related negativity
Eligibility Criteria
Inclusion Criteria:
- Children between ages 4 -5.99 years at time of consent
- Children that have a primary clinical diagnosis of separation anxiety disorder, social anxiety disorder, generalized anxiety disorder, panic disorder, and/or obsessive-compulsive disorder
- Written informed consent by a parent/legal guardian and verbal assent from participant
- Fluent in English
Exclusion Criteria:
- History of head injury
- History of serious medical or neurological illness
- History of post-traumatic stress disorder (PTSD)
- History of major depressive disorder (MDD)
- Current psychotherapy or behavioral interventions
- History of Neurodevelopmental delay, autism spectrum disorder (ASD), or intellectual disability
- Currently taking medications that affect central nervous system functioning
- Primary clinical diagnosis is selective mutism or specific phobia
- Recent history of physically aggressive behaviors that have caused harm to other children
- Sibling of a child who has participated or is currently participating in this protocol
Sites / Locations
- University of Michigan
- Michigan State UniversityRecruiting
- New York State Psychiatric Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Kidpower - Structured Games
Kidpower - Playgroup
Arm Description
Structured Games Camp.
Playgroup camp
Outcomes
Primary Outcome Measures
Change in Error Related Negativity (ERN)
The error-related negativity is a neurophysiological signal, measured via electroencephalogram (EEG), considered to reflect a dorsal anterior cingulate cortex (ACC) response to errors. For this study the ERN will be measured at electrode site FCz as the downward (negative voltage) deflection of the EEG signal that occurs 50-100 msec after error commission on the Zoo Task. Scores are measured continuously (no established minimum or maximum) . Higher scores reflect greater neural capacity for effortful control.
Change in National Institutes of Health (NIH) Toolbox Effortful Control (EC) Composite Scale
The NIH Toolbox EC Composite Scale will be comprised of children's standardized scores reflecting accuracy and reaction time on two computerized tasks: the Flanker inhibitory control and attention task and the Dimensional Change Card Sort (DCCS) test of set-shifting function. An NIH Toolbox EC Composite score will be based on factor loadings for each task derived from a factor analysis of scores across both Toolbox tasks. Scores are measured continuously (no established minimum or maximum) . Higher scores reflect greater behavioral capacity for effortful control.
Change in Clinical Global Impressions -Severity and Improvement Scales
The Clinical Global Impressions (CGI) is an observer rated scale used to assess anxiety severity (CGI-S) and pre- to post-treatment improvement in anxiety (CGI-I). Ratings for both use a 7-point scale, from 1 "normal" to 7 "among the most severely ill" for CGI-S and 1 ("very much improved") to 7 ("very much worse") for CGI-I.
Secondary Outcome Measures
Change in Anxiety Disorders Interview Schedule - Parent Version (ADIS-P)
ADIS-P is a semi-structured clinical interview administered to parents to assess Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) diagnoses where anxiety is a component. Severity of symptoms is rated by interviewers on a scale from none (=0) to very severe (=8), with clinician severity rating (CSR) ≥ 4 indicating presence of diagnosis.. Changes in CSR of the primary (i.e., most severe at baseline) anxiety diagnosis from pre to post intervention will be assessed.
Change in Spence Preschool Anxiety Scale (Spence PAS)
The Spence PAS is a validated instrument for the measurement of parent report of anxiety symptoms in young children. Spence PAS scores will provide a continuous rating of anxiety symptoms from 0 to 112; high scores reflect greater anxiety.
Full Information
NCT ID
NCT04960813
First Posted
July 2, 2021
Last Updated
August 11, 2023
Sponsor
Columbia University
Collaborators
National Institute of Mental Health (NIMH), Michigan State University, University of Michigan, University of Maryland
1. Study Identification
Unique Protocol Identification Number
NCT04960813
Brief Title
Kidpower Camp - Structured Games or Playgroup
Official Title
Neurally Targeted Interventions to Reduce Early Childhood Anxiety
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 7, 2021 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
National Institute of Mental Health (NIMH), Michigan State University, University of Michigan, University of Maryland
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Clinically significant anxiety affects 20% of preschoolers and can become chronic, leading to depression, substance abuse, school-drop out and even suicide. To reduce anxiety and prevent its sequelae, clinically affected children must be effectively treated early. Available interventions for clinically anxious preschoolers are effective for some, but not all children, with as many as 50% of 4-7 year olds continuing to meet criteria for an anxiety disorder after treatment.
This trial aims to help learn how Camp Kidpower, trainings using either structured games or a playgroup, may lower anxiety in preschool age children. Playing these games and learning that kids can do it, can teach kids how to keep going when they are feeling anxious. To find out if Kidpower works by helping kids stay in charge of their behaviors and emotions, the study will look at parts of the brain as well as behaviors related to effortful control and fear, before and after training.
The study hypothesizes that Kidpower will produce greater increases in Error-related negativity (ERN), Interchannel Phase Synchrony (ICPS) and effortful control (EC) behaviors than in the Playgroup control.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Disorders
Keywords
Effortful Control, Preschool, Error-related negativity
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Children and one legal guardian/primary caregiver will be randomized 1:1 to structured games or a playgroup. The structured games and playgroup will run in parallel.
Masking
Outcomes Assessor
Masking Description
The rater will be blinded to which intervention, structured games or playgroup, child participants receive.
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Kidpower - Structured Games
Arm Type
Experimental
Arm Description
Structured Games Camp.
Arm Title
Kidpower - Playgroup
Arm Type
Active Comparator
Arm Description
Playgroup camp
Intervention Type
Behavioral
Intervention Name(s)
Structured games
Intervention Description
Camp Kidpower - Structured Games is an interactive, child-friendly "camp" and is comprised of short, game-like exercises taught by "camp counselors" to groups of approximately 4-6 children. In total, 15 different exercises will be taught. Children will attend 5 three-hour playgroup sessions over a 4-week period (twice the first week, and then only once per week for the subsequent 3-week period) to match the Playgroup intervention.
Parents will be asked to attend an approximately one-hour group meeting, during which information is presented regarding child anxiety, effortful control and the rationale for this treatment. Parents are asked to continue to utilize the intervention at home every day if possible with the child and will receive texts or emails to track the games that are played at home.
Intervention Type
Behavioral
Intervention Name(s)
Playgroup
Intervention Description
Camp Kidpower - Playgroup includes structured play activities. This will include art activities, dramatic play props, and a "story time". Children will attend 5 three-hour playgroup sessions over a 4-week period (twice the first week, and then only once per week for the subsequent 3-week period) to match the Kidpower intervention.
During the first week parents will attend an approximately one-hour group meeting, during which information is presented regarding the positive benefits of child-led play and "special time" with caregivers.
Parents well be asked to complete homework with their children during the week between sessions, and are shown how to track time spent in this activity. Parents will receive a daily text (or email) to to measure frequency of homework practice between sessions.
Primary Outcome Measure Information:
Title
Change in Error Related Negativity (ERN)
Description
The error-related negativity is a neurophysiological signal, measured via electroencephalogram (EEG), considered to reflect a dorsal anterior cingulate cortex (ACC) response to errors. For this study the ERN will be measured at electrode site FCz as the downward (negative voltage) deflection of the EEG signal that occurs 50-100 msec after error commission on the Zoo Task. Scores are measured continuously (no established minimum or maximum) . Higher scores reflect greater neural capacity for effortful control.
Time Frame
Pre-treatment (baseline) and post-treatment assessments (approximately 4-6 weeks)
Title
Change in National Institutes of Health (NIH) Toolbox Effortful Control (EC) Composite Scale
Description
The NIH Toolbox EC Composite Scale will be comprised of children's standardized scores reflecting accuracy and reaction time on two computerized tasks: the Flanker inhibitory control and attention task and the Dimensional Change Card Sort (DCCS) test of set-shifting function. An NIH Toolbox EC Composite score will be based on factor loadings for each task derived from a factor analysis of scores across both Toolbox tasks. Scores are measured continuously (no established minimum or maximum) . Higher scores reflect greater behavioral capacity for effortful control.
Time Frame
Pre-treatment (baseline) and post-treatment assessments (approximately 4-6 weeks)
Title
Change in Clinical Global Impressions -Severity and Improvement Scales
Description
The Clinical Global Impressions (CGI) is an observer rated scale used to assess anxiety severity (CGI-S) and pre- to post-treatment improvement in anxiety (CGI-I). Ratings for both use a 7-point scale, from 1 "normal" to 7 "among the most severely ill" for CGI-S and 1 ("very much improved") to 7 ("very much worse") for CGI-I.
Time Frame
Pre-treatment (baseline) and post-treatment assessments (approximately 4-6 weeks)
Secondary Outcome Measure Information:
Title
Change in Anxiety Disorders Interview Schedule - Parent Version (ADIS-P)
Description
ADIS-P is a semi-structured clinical interview administered to parents to assess Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) diagnoses where anxiety is a component. Severity of symptoms is rated by interviewers on a scale from none (=0) to very severe (=8), with clinician severity rating (CSR) ≥ 4 indicating presence of diagnosis.. Changes in CSR of the primary (i.e., most severe at baseline) anxiety diagnosis from pre to post intervention will be assessed.
Time Frame
Pre-treatment (baseline) and post-treatment assessments (approximately 4-6 weeks)
Title
Change in Spence Preschool Anxiety Scale (Spence PAS)
Description
The Spence PAS is a validated instrument for the measurement of parent report of anxiety symptoms in young children. Spence PAS scores will provide a continuous rating of anxiety symptoms from 0 to 112; high scores reflect greater anxiety.
Time Frame
Pre-treatment (baseline) up to post-treatment assessments (approximately 4-6 weeks)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
48 Months
Maximum Age & Unit of Time
71 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Children between ages 4 -5.99 years at time of consent
Children that have a primary clinical diagnosis of separation anxiety disorder, social anxiety disorder, generalized anxiety disorder, panic disorder, and/or obsessive-compulsive disorder
Written informed consent by a parent/legal guardian and verbal assent from participant
Fluent in English
Exclusion Criteria:
History of head injury
History of serious medical or neurological illness
History of post-traumatic stress disorder (PTSD)
History of major depressive disorder (MDD)
Current psychotherapy or behavioral interventions
History of Neurodevelopmental delay, autism spectrum disorder (ASD), or intellectual disability
Currently taking medications that affect central nervous system functioning
Primary clinical diagnosis is selective mutism or specific phobia
Recent history of physically aggressive behaviors that have caused harm to other children
Sibling of a child who has participated or is currently participating in this protocol
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Caroline Risdon, B.S.
Phone
646-774-5868
Email
caroline.risdon@nyspi.columbia.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Berenis Baez
Email
bb2145@cumc.columbia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kate D Fitzgerald, M.D.
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Individual Site Status
Completed
Facility Name
Michigan State University
City
East Lansing
State/Province
Michigan
ZIP/Postal Code
48824
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jason S Moser, Ph.D.
Phone
517-355-2159
Email
jmoser@msu.edu
First Name & Middle Initial & Last Name & Degree
Jason S Moser, Ph.D.
Facility Name
New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Individual Site Status
Suspended
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Kidpower Camp - Structured Games or Playgroup
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