Evaluating the Results of Physician and Parent Decisions to Treat Selective Mutism With Fluoxetine
Primary Purpose
Selective Mutism, Social Anxiety
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Fluoxetine
Sponsored by
About this trial
This is an interventional treatment trial for Selective Mutism focused on measuring Selective Mutism, Social Anxiety, Children, Adolescents
Eligibility Criteria
Inclusion Criteria:
- Male or female from seven to seventeen years of age at their last birthday
- Meet DSM-IV-TR criteria for selective mutism
- No history of medication treatment for selective mutism
- Child has an immediate biological family member who is diagnosed with an anxiety disorder or has experienced symptoms of an anxiety disorder at some point in time
- Child has received 10 weeks of an evidence-based psychosocial treatment
- Child has never had a negative reaction to a psychopharmacological medication
- Child exhibits symptoms of social anxiety
Exclusion Criteria:
- Child is diagnosed with a speech condition, mental retardation, pervasive developmental disorder, or schizophrenia
- Child is an English language learner or from a different culture than the culture predominately represented within his or her school
- Child is taking or has taken any kind of a psychopharmacological medication (e.g., SSRI, MAO-I, stimulant, etc.)
- Child has a medical illness that may be complicated through the use of a psychopharmacological treatment
Sites / Locations
- Michigan State University Psychiatry Clinic
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Fluoxetine
Arm Description
Children will receive an introductory dose and therapeutic dose of fluoxetine at various time points in the study. Onset of fluoxetine is determined by assignment to a pre-determined randomized treatment schedule.
Outcomes
Primary Outcome Measures
Selective Mutism Questionnaire (Change Over 15 Weeks)
Secondary Outcome Measures
Multidimensional Anxiety Scale for Children - 2nd Edition (Change Over 15 Weeks)
Direct Behavior Ratings - Parent (Change Over 15 Weeks)
Clinical Global Impression (Change Over 15 Weeks)
Side Effects Form for Children and Adolescents - Adapted (Change Over 15 Weeks)
Parent - Young Mania Rating Scale (Change Over 15 Weeks)
Treatment Evaluation Questionnaire - Parent
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05378711
Brief Title
Evaluating the Results of Physician and Parent Decisions to Treat Selective Mutism With Fluoxetine
Official Title
Evaluating the Results of Physician and Parent Decisions to Treat Selective Mutism With Fluoxetine
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
January 1, 2014 (Actual)
Primary Completion Date
May 30, 2015 (Actual)
Study Completion Date
May 30, 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Michigan State University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The Department of Counseling, Educational Psychology, and Special Education and the Department of Psychiatry at Michigan State University have coordinated efforts to provide a diagnostic and treatment investigation for children, ages seven to eighteen, with Selective Mutism. The purpose of this study is to examine the utility of fluoxetine for the treatment of this debilitating disorder. Fluoxetine is expected to improve social anxiety and selective mutism symptomology.
Detailed Description
Children with selective mutism (SM) are at risk for current and continuing academic and socio-emotional difficulties. Unfortunately, this issue is complicated by the fact these children often respond poorly to psychosocial intervention. This leaves parents with the overwhelming decision to attempt a trial of medication regardless of the little available data on the evidence base of this approach. Despite the paucity of research, psychiatrists are prescribing fluoxetine for children with SM "off label", as the Food and Drug Administration (FDA) has yet to approve fluoxetine for this indication. This study blends the psychopharmacological expertise of psychiatrists with the mental health, systems, and psychological evaluation expertise of school psychologists to identify an appropriate psychopharmacological solution for children and adolescents with this debilitating disorder. To that end, this study will examine the utility of fluoxetine for the treatment of five children and adolescents, ages seven to eighteen, diagnosed with SM through the use of a non-concurrent multiple-baseline single-case design with a single-blind placebo-controlled procedure. Treatment effectiveness will be evaluated by visual analysis of the data, the Wampold and Worsham multiple-baseline design randomization test, and the Kendall's Tau + Mann-Whitney U effect size. Multiple methods of assessment including standardized measures, such as the Selective Mutism Questionnaire (SMQ), and behavior ratings, such as Direct Behavior Ratings (DBRs), will be used to gather baseline and treatment data. Multiple informants (i.e., parents, teachers, and psychiatrists) will provide information on treatment effect across settings (i.e., school and community). Information regarding adverse effects associated with fluoxetine treatment including a measure of behavioral disinhibition, parental acceptance of the fluoxetine intervention, and compliance with taking the medication will also be gathered.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Selective Mutism, Social Anxiety
Keywords
Selective Mutism, Social Anxiety, Children, Adolescents
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
Double
Masking Description
Participants serve as their own controls by being randomly assigned to switch from placebo to active medication at staggered start dates per single case design methodology.
Allocation
N/A
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Fluoxetine
Arm Type
Experimental
Arm Description
Children will receive an introductory dose and therapeutic dose of fluoxetine at various time points in the study. Onset of fluoxetine is determined by assignment to a pre-determined randomized treatment schedule.
Intervention Type
Drug
Intervention Name(s)
Fluoxetine
Other Intervention Name(s)
Prozac
Intervention Description
Children will receive a placebo or fluoxetine at different times dependent upon random assignment to a treatment schedule.
Primary Outcome Measure Information:
Title
Selective Mutism Questionnaire (Change Over 15 Weeks)
Time Frame
2 times per week for 15 weeks
Secondary Outcome Measure Information:
Title
Multidimensional Anxiety Scale for Children - 2nd Edition (Change Over 15 Weeks)
Time Frame
2 times per week for 15 weeks
Title
Direct Behavior Ratings - Parent (Change Over 15 Weeks)
Time Frame
Parent (3 times per week for 15 weeks); Teacher (5 times per week for 15 weeks)
Title
Clinical Global Impression (Change Over 15 Weeks)
Time Frame
Parent and Teacher (2 times per week for 15 weeks); Psychiatrist (biweekly for 15 weeks)
Title
Side Effects Form for Children and Adolescents - Adapted (Change Over 15 Weeks)
Time Frame
biweekly for 15 weeks
Title
Parent - Young Mania Rating Scale (Change Over 15 Weeks)
Time Frame
2 times per week for 15 weeks
Title
Treatment Evaluation Questionnaire - Parent
Time Frame
End of Study (after 15 weeks)
Other Pre-specified Outcome Measures:
Title
Treatment Integrity Form
Time Frame
Daily for 15 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female from seven to seventeen years of age at their last birthday
Meet DSM-IV-TR criteria for selective mutism
No history of medication treatment for selective mutism
Child has an immediate biological family member who is diagnosed with an anxiety disorder or has experienced symptoms of an anxiety disorder at some point in time
Child has received 10 weeks of an evidence-based psychosocial treatment
Child has never had a negative reaction to a psychopharmacological medication
Child exhibits symptoms of social anxiety
Exclusion Criteria:
Child is diagnosed with a speech condition, mental retardation, pervasive developmental disorder, or schizophrenia
Child is an English language learner or from a different culture than the culture predominately represented within his or her school
Child is taking or has taken any kind of a psychopharmacological medication (e.g., SSRI, MAO-I, stimulant, etc.)
Child has a medical illness that may be complicated through the use of a psychopharmacological treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jed Magen, DO
Organizational Affiliation
Michigan State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John Carlson, PhD
Organizational Affiliation
Michigan State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Justin Barterian, MA
Organizational Affiliation
Michigan State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Joel Sanchez, MD
Organizational Affiliation
Michigan State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Michigan State University Psychiatry Clinic
City
East Lansing
State/Province
Michigan
ZIP/Postal Code
48824
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Evaluating the Results of Physician and Parent Decisions to Treat Selective Mutism With Fluoxetine
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