- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00136279
Linking Lives: Building Quality Parent Components for School-Based Health Programs in Middle Schools
RCT of Tobacco Use Prevention and Sexual Risk Reduction Interventions for Parents of African American and Latino Youth in Middle School
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Although parent-based programs have shown promise in reducing adolescent risk behavior, few have been rigorously evaluated and shown to be effective. Recruitment and retention of parents into lengthy workshops has been a problem and few programs have been developed specifically for inner-city, minority populations who are at greatest risk for a number of adverse health outcomes. Linking Lives was designed to address these issues.
Parent Intervention. The primary feature of the parent component is a written manual distributed in modules to mothers that teaches them how to communicate effectively with their children about sex or tobacco risk behaviors and how to improve their relationships with their children. This is accompanied by two face-to-face intervention sessions for mothers, during which they are given the intervention materials and an opportunity to participate in role playing activities with other parents, and by regular contact by trained parent volunteers to determine if the parent has implemented the manual contents. Mothers and their adolescents attend Linking Lives events together at the school in the evenings and on weekends during which time adolescents attend their own intervention sessions at the same time mothers are attending theirs (mothers in the control condition participate in sessions on helping their children choose a high school).
Sample. Nine middle schools in the Bronx, New York and two schools in the Harlem neighborhood of New York are participating in the study. The schools are located in communities that are financially disadvantaged. Approximately 70% of the students in the schools are Latino and 30% are African American. A total of 4,750 adolescents and their mothers will participate in the study, 1,900 for tobacco and 2,850 for sexual risk reduction. Students are randomly sampled and their parent is contacted regarding family participation in the study.
Evaluation. Based on input from elicitation studies, focus groups with adolescents and mothers, a pre-intervention survey of 668 mother-adolescent pairs, a psychometric study for both English- and Spanish-language instruments, feedback from community and school leaders, and a scientific panel of experts, the instruments, manuals and intervention protocol have been developed. All measures and intervention materials have been developed in English and in Spanish. The evaluation includes a baseline, 3-month post-test and a 15-month delayed post-test assessment of adolescents and mothers. For tobacco, within schools, students will be randomly assigned to an experimental group (school-based curriculum plus parent component) or a control group (school-based curriculum only). For sexual risk reduction, students will be randomly assigned to the combined experimental condition (school-based curriculum plus parent component), a parent-only experimental condition (parent component is distributed to mothers, but no school component is delivered) or a control group (school-based curriculum only).
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
New York, New York, United States, 10027
- Columbia University School of Social Work
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- African American or Latino
- 6th or 7th grade students
- Residential mothers or primary female caregivers
Exclusion Criteria:
- 8th grade students
- Fathers or primary male caregivers
Study Plan
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: School plus parent
Adolescents receive school-based curriculum (either Project TNT or Making a Difference) and mothers receive the Linking Lives curriculum
|
Parent intervention consists of mothers attending two, 2.5 hour-long, face-to-face sessions at the school during which they are given an intervention manual, two homework assignments, and a manual for their adolescent.
Parents also receive two booster telephone calls approximately one-month and six-months after completing the intervention.
As part of the comparison condition, school-based interventions for adolescents also consist of two, 2.5 hour-long, face-to-face sessions at schools during which they complete either the Project TNT intervention for preventing tobacco use or the Making a Difference intervention for reducing sexual risk behavior.
|
Active Comparator: School-only
Adolescents receive school-based curriculum and parents received a control curriculum on helping their child choose a high school
|
Parent intervention consists of mothers attending two, 2.5 hour-long, face-to-face sessions at the school during which they are given an intervention manual, two homework assignments, and a manual for their adolescent.
Parents also receive two booster telephone calls approximately one-month and six-months after completing the intervention.
As part of the comparison condition, school-based interventions for adolescents also consist of two, 2.5 hour-long, face-to-face sessions at schools during which they complete either the Project TNT intervention for preventing tobacco use or the Making a Difference intervention for reducing sexual risk behavior.
|
Experimental: Parent-Only
In the sex risk reduction portion of the study only, a second experimental group consisted of parents receiving the Linking Lives intervention and adolescents receiving no in-school intervention
|
Parent intervention consists of mothers attending two, 2.5 hour-long, face-to-face sessions at the school during which they are given an intervention manual, two homework assignments, and a manual for their adolescent.
Parents also receive two booster telephone calls approximately one-month and six-months after completing the intervention.
As part of the comparison condition, school-based interventions for adolescents also consist of two, 2.5 hour-long, face-to-face sessions at schools during which they complete either the Project TNT intervention for preventing tobacco use or the Making a Difference intervention for reducing sexual risk behavior.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Self-reported ever had sex or ever smoked a cigarette
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Intentions to have sex or to smoke cigarettes
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Age at first intercourse or first cigarette
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Condom use at last sex
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Contraceptive use at last sex
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Maternal monitoring and supervision
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Maternal Communication about smoking cigarettes or sexual intercourse
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Quality of maternal communication
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Self-reported regular cigarette smoking
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Intentions to smoke marijuana
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Ever smoked marijuana
Time Frame: 3-month and 15-month follow-up
|
3-month and 15-month follow-up
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Vincent Guilamo-Ramos, PhD, Columbia University
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CDC-NCCDPHP-3486
- U87/CCU220155-05
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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