Anxiety Clinical Trial
— TAPESOfficial title:
Teacher Anxiety Program for Elementary Students
Verified date | September 2022 |
Source | UConn Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the study is to compare two teacher trainings developed to assist elementary students who struggle with excessive anxiety. The goal of both teacher trainings is to improve teachers' knowledge and skills for identifying and assisting students with excessive anxiety. The first training program is called TAPES (Teacher Anxiety Program for Elementary Students) and involves a 6 hour teacher training. Teachers in this training program will implement anxiety reduction skills in the classroom and complete 5 brief (approximately 30 minute) meetings with the student and his or her parent(s)/guardian(s). The second training program, Teacher Anxiety Training (TAT), involves a 3 hour teacher training. Teachers in the TAT condition learn to implement anxiety reduction skills in the classroom, but do not conduct individual meetings with parents and students. The investigators do not know if TAT and TAPES work equally well, or if one is better than the other. Both will be administered by teachers to see if they help youth with excessive anxiety feel less worried.
Status | Completed |
Enrollment | 54 |
Est. completion date | June 30, 2022 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 5 Years to 12 Years |
Eligibility | Inclusion Criteria: - Must attend a CT elementary school - Must have elevated anxiety symptoms, which is defined as a total Spence Children's Anxiety Scale t score > 60 based on parent and/or child report and/or a Clinician Severity Rating (CSR) of 3 or greater on the Anxiety Disorder Interview Schedule (ADIS-V). Exclusion Criteria: - Any medical or psychiatric condition contraindicating the study participation (based on clinical interview; such as recent suicidality) |
Country | Name | City | State |
---|---|---|---|
United States | University of Connecticut Health Center | West Hartford | Connecticut |
Lead Sponsor | Collaborator |
---|---|
UConn Health |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from Baseline on the Teacher Knowledge Assessment | Two equivalent forms assessing teachers' knowledge of anxiety symptoms and anxiety-reduction strategies. Comprised of multiple-choice and short-answer questions. | Baseline, 8 week Post-Intervention | |
Primary | Change from Baseline on the Classroom Observation of Teachers Skills | This is a form created for this study that is completed by two independent evaluators following direct observations of teachers. Observers rate the teachers' use of teaching behaviors reviewed in the training. Scores are generated for 3 domains: Teacher behaviors that may decrease anxiety (Do Behaviors), behaviors that may increase anxiety (Don't Behaviors), and behaviors that evidence strong teacher-student relationships (Relationship Behaviors). Teachers are rated on a 5 point Likert-type scale, with 0 indicating poor behavior and 4 indicating very good or excellent behavior (min score = 0, max score = 4 on all domains). There is no combined total score. Higher values in each domain demonstrate greater mastery of teaching behaviors reviewed in the training. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Modified Anxiety Diagnostic Interview Schedule, for the Diagnostic and Statistical Manual Fifth Edition (ADIS-V) | Semi-structured clinical interview assessing student anxiety diagnosis and severity. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Spence Children's Anxiety Scale, Child and Parent Versions | The Spence Children's Anxiety Scale is a reliable and valid measure of anxiety symptoms in children. Both versions use a 4-point Likert scale to assess frequency of symptoms (0 = never, 3 = always). The child report has 44 items--38 of which are used to calculate the total score. The parent report has a total of 39 items--38 of which are used in the total score (minimum score 0 , maximum score 114). On both forms, higher scores represent higher levels of anxiety. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Child Anxiety Impact Scale, Child and Parent Versions (& adapted Teacher Version) | The Child Anxiety Impact Scale measures the impact of a child's anxiety across school, home, and social domains. Both versions use a 4-point Likert scale (0 = not at all, 3 = very much) to assess the frequency of anxiety impairment in various areas. The range for the total score is 0 (minimum) to 81 (maximum). Subscale scores range from a minimum of 0 to a maximum of 30, 33, and 18 for the school, social, and home subscales, respectively. Higher scores represent greater interference of anxiety in child functioning. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Woodcock Johnson IV Tests of Achievement (Fluency subtests) | Psychometrically validated measure of academic fluency in children. Scores are generated as standard scores with a mean of 100 and a standard deviation of 15. Higher scores represent better academic performance. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Woodcock Johnson IV Tests of Cognitive Abilities (Numbers Reversed subtest) | Psychometrically validated measure of working memory in children. Scores are generated as standard scores with a mean of 100 and a standard deviation of 15. Higher scores represent better working memory capacity. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Family Accommodation Scale, Anxiety (FASA) Parent form (& adapted teacher version) | Measures frequency of parent (and teacher) accommodation behaviors in relation to child's anxiety symptoms. Items are rated on a 5-point Likert scale (0 = Never, 4 = Daily). Items 1-9 are summed to find total accommodation behaviors (minimum score = 0, maximum score = 36). Higher scores represent more accommodation behaviors associated with more anxiety-related impairment in family functioning or classroom functioning. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Children's Global Assessment Scale (CGAS) | The Children's Global Assessment Scale is a single-item measure of child's overall behavioral functioning assigned by a clinical interviewer. Scores on this scale range from 1 to 100. Higher scores are associated with more adaptive functioning. More specifically, scores below 70 are indicative of increasingly severe impairment in behavioral functioning. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the Clinical Global Impression - Severity (CGI-S) and Improvement (CGI-I) Scales | These two single-item scales measure a student's anxiety symptom severity and improvement as rated by a clinical interviewer. On the Severity scale, scores range from 1 (Normal) to 7 (Extremely Ill). Higher scores represent greater anxiety symptom severity. On the Improvement scale, scores range from 1 (Very Much Improved) to 7 (Very Much Worse). Lower scores represent better outcomes relative to the baseline assessment. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up | |
Secondary | Change from Baseline on the School Anxiety Scale | The School Anxiety Scale is a teacher-report measure of anxiety symptoms exhibited in the classroom. This 16-item measure uses a 4-point Likert scale to measure the frequency of anxiety-related behaviors (0 = never, 3 = always). The scale has a minimum score of 0, and a maximum score of 48. Higher scores represent more frequent anxiety-related behaviors in the classroom. | Baseline, 8-week post-intervention, 3-month post-intervention follow-up |
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