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Clinical Trials/NCT00459238
NCT00459238
Completed
Not Applicable

A Telephone-Based Education and Prevention Intervention for Teens and Young Adults

Georgetown University1 site in 1 country104 target enrollmentOctober 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Unspecified Childhood Solid Tumor, Protocol Specific
Sponsor
Georgetown University
Enrollment
104
Locations
1
Primary Endpoint
Knowledge
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

RATIONALE: Telephone-based cancer education and counseling may help participants learn about ways of preventing cancer and choose a lifestyle that will help them stay healthy as they grow older.

PURPOSE: This randomized clinical trial is studying telephone-based cancer education and telephone-based counseling to see how well they work compared with telephone-based cancer education alone in young participants.

Detailed Description

OBJECTIVES: Primary * Compare the efficacy of telephone-based cancer education with vs without counseling in younger participants. Secondary * Determine the mechanisms by which education with counseling may impact cancer-relevant cognitive and behavioral outcomes. * Identify teens who may be most and least likely to benefit from education with counseling. OUTLINE: This is a pilot, controlled, randomized study. Participants are stratified according to age (13-14 years vs 15 years vs 16 years vs 17 years vs 18-21 years), gender, race (white vs black vs other), and health status (chronic disease vs no chronic disease). Participants are randomized to 1 of 2 education arms. * Arm I: Participants undergo cancer education sessions via telephone over 45 minutes once a week for 8 weeks. * Arm II: Participants under cancer education sessions as in arm I and counseling techniques during the same telephone sessions. In both arms, participants receive an intervention kit by mail before the first telephone call. The intervention kit includes age-appropriate self-help materials. PROJECTED ACCRUAL: A total of 300 participants will be accrued for this study.

Registry
clinicaltrials.gov
Start Date
October 2006
End Date
December 2010
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Knowledge

Time Frame: 6 months

Tobacco use intentions and behavior

Time Frame: 6 months

Screening intentions

Time Frame: 6 months

Health history taking

Time Frame: 3 months

Nutrition

Time Frame: 6 months

Multiple risk factor index

Time Frame: 6 months

Physical activity

Time Frame: 6 months

Perceived benefits

Time Frame: 6 months

Perceived barriers

Time Frame: 6 months

Alcohol use intentions and behavior

Time Frame: 6 months

Self-efficacy

Time Frame: 6 months

Study Sites (1)

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