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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00136279
Other study ID # CDC-NCCDPHP-3486
Secondary ID U87/CCU220155-05
Status Completed
Phase N/A
First received August 25, 2005
Last updated January 30, 2009
Start date January 2004
Est. completion date September 2007

Study information

Verified date January 2009
Source Centers for Disease Control and Prevention
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to develop and evaluate the effectiveness of a parent-based intervention that can be implemented in conjunction with existing school-based programs designed to prevent or reduce sexual risk behavior or to prevent or reduce tobacco use in young adolescents. The parent programs are expected to have effects on adolescent behavior over and above the effects of the school-based programs.


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).


Recruitment information / eligibility

Status Completed
Enrollment 9510
Est. completion date September 2007
Est. primary completion date September 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility 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 Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Behavioral:
Linking Lives parent-based 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.

Locations

Country Name City State
United States Columbia University School of Social Work New York New York

Sponsors (2)

Lead Sponsor Collaborator
Centers for Disease Control and Prevention Columbia University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Self-reported ever had sex or ever smoked a cigarette 3-month and 15-month follow-up No
Secondary Intentions to have sex or to smoke cigarettes 3-month and 15-month follow-up No
Secondary Age at first intercourse or first cigarette 3-month and 15-month follow-up No
Secondary Condom use at last sex 3-month and 15-month follow-up No
Secondary Contraceptive use at last sex 3-month and 15-month follow-up No
Secondary Maternal monitoring and supervision 3-month and 15-month follow-up No
Secondary Maternal Communication about smoking cigarettes or sexual intercourse 3-month and 15-month follow-up No
Secondary Quality of maternal communication 3-month and 15-month follow-up No
Secondary Self-reported regular cigarette smoking 3-month and 15-month follow-up No
Secondary Intentions to smoke marijuana 3-month and 15-month follow-up No
Secondary Ever smoked marijuana 3-month and 15-month follow-up No
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