Middle School Matters Study

Depression Clinical Trial

— MSM  

Official title:

Prevention of Depression Within Salient Adolescent Contexts

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01220635
• Other study ID #: R34 MH083706
• Secondary ID: 5R34MH083076-03
• Status: Completed
• Phase: N/A
• First received: October 5, 2010
• Last updated: February 13, 2014
• Start date: October 2010
• Est. completion date: October 2012

Study information

• Verified date: February 2014
• Source: Seattle Children's Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

This study aims to evaluate the short-term and long-term efficacy of two preventative intervention approaches designed to support middle school youth.

Description:

This study involve two parts: Part 1 entailed screening 7th and 8th graders from 4 public middle schools to identify students who may be showing moderate signs of stress. Students who score at the designated cutoff on a depression symptoms measure received a brief check-in to determine eligibility for the follow up randomized trial (Part 2). An "indicated" sample of 120 adolescents in the 7th and 8th grade and their caregivers were randomly assigned to a brief, Individual Support Program (ISP) comparison group or a Skills Group Program. Research interviews were conducted at multiple timepoints with students and caregivers, and teacher questionnaires were used to examine changes in outcome measures. Following completion of the intervention, all participants were followed for 12-months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 120
• Est. completion date: October 2012
• Est. primary completion date: October 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• 7th and 8th grade students at 4 participating middle schools

• Score 14 or above on the Mood and Feelings Questionnaire at screening (approximately top 25%)

• No imminent plans to move or change to non-participating school

• At minimum 6th grade language skills

• Agree to participate in random assignment and research interviews

• One Parent/caregiver willing to complete research interviews

Exclusion Criteria:

• Student with past or current Major Depressive Disorder (MDD) or Probable MDD

• Students with parents who do not speak English or Spanish

• Students in concurrent treatment

• Students in self-contained classroom, or with cognitive delays, or emotional behavioral problems that would preclude them from benefiting from the group or being a good group member

• Parent not willing to complete research interviews

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Depression
• Depressive Disorder

Intervention

Behavioral:
• Positive Thoughts and Actions Program
Students in the skills group will attend a 12-session (50 minutes each), 12-week program with 4-6 other students. The skills group will take place at school during school hours. Parents in the skill group will be asked to participate in two parent group workshops to take place at their child's school or other participating middle school (2-hours each). In addition, the skill group leader will conduct two individual family meetings with the student and parent(50 minutes each).
• Individual Support Program
Students will be individually interviewed (60-90 minutes) at school to review areas of stress and support. The health professional conducting the interview will reinforce the student's strengths, and provide connections to sources of help from caring adults at home and at school. Parents will be called following the assessment to help the family locate appropriate resources if needed (e.g., tutoring resources, school counselor).

Locations

Country	Name	City	State
United States	Seattle Children's	Seattle	Washington

Sponsors (2)

Lead Sponsor	Collaborator
Seattle Children's Hospital	National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Moods and Feelings Questionnaire (MFQ; child and parent version)	Depressive symptoms of the child are assessed on the MFQ. Youth completed the MFQ at all 4 timepoints, parent ratings of students symptoms were collected at baseline, post-intervention, and 12 month follow up.	up to 1 year	No
Secondary	Parent-Child Communication (PCC; child and parent version)	Parent child communication were assessed using the child and parent version of the PCC. Children completed the PCC at all 4 timepoints, parent ratings were collected at baseline, post-intervention, and 12 month follow up.	up to 1 year	No
Secondary	Behavioral Assessment System for Children-2nd Edition (BASC-2; student, parent, & teacher version)	The adolescent version of the Teacher Rating Scale, Parent Rating Scale, and the Student Self-Report of Personality of the BASC-2 were used to assess school functioning and social functioning.	up to 1 year	No
Secondary	Health Enhancing Behavior Index (HEBI)	Health behaviors (diet, exercise, and sleep) are self-reported by the youth on the HEBI.	up to 1 year	No
Secondary	Service Use Interview (Service for Children and Adolescence Parent Interview-modified)	The service use interview was used to measure treatment history and services received during the course of the intervention and follow up.	up to 1 year	No
Secondary	Schedule for Affective Disorders and Schizophrenia for School-Age Children (KSADS)	The depression module of the KSADS was used to assess DSM-IV symptoms of major depression and depressive disorder at the 12-month follow up.	up to 1 year	No