Overview

This trial is active, not recruiting.

Conditions cancer, risk factors in latinos
Treatments questionnaires, accelerometer, smart phone
Sponsor M.D. Anderson Cancer Center
Collaborator National Cancer Institute (NCI)
Start date January 2012
End date January 2022
Trial size 225 participants
Trial identifier NCT01479257, 1K01CA157689, 2011-0696, R25T CA57730

Summary

The goal of this research study is to learn how cultural, environmental, and interpersonal experiences, as well as personal thoughts and feelings, influence cancer risk behaviors among Latino residents of Houston, Texas.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective
Arm
Bilingual Houston area Latinos surveyed for 7 continuous days with objective and subjective assessments using accelerometer and smart phone.
questionnaires Surveys
36 questionnaires at the first visit (a total of 474 questions) and 25 questionnaires at the second visit (a total of 278 questions), taking about 60 to 90 minutes to complete each visit.
accelerometer Movement meter
Small device worn on the hip for 7 consecutive days that measures physical activity.
smart phone cell phone
Questions on smart phone up to 5 times a day for 7 days taking about 5-7 minutes to complete each time.

Primary Outcomes

Measure
Determinants of Cancer Risk Behaviors in Latinos
time frame: 7 days

Eligibility Criteria

Male or female participants from 18 years up to 65 years old.

Inclusion Criteria: 1. Self-identify as Latino in ethnicity 2. Are between the ages of 18-65, inclusive 3. Possess a valid home address and functioning telephone number 4. Possess marginal to adequate health literacy in English (as indicated by a score of at least 45 on the Rapid Estimate of Adult Literacy in Medicine) and Spanish (as indicated by a score of at least 38 on the Short Assessment of Health Literacy for Spanish Adults). Exclusion Criteria: 1. Used an illicit substance in the past 30 days 2. Another household member enrolled in the study 3. Pregnant or breastfeeding 4. Participated in a smoking cessation program in the last 90 days 5. Uses nicotine replacement products 6. Uses other tobacco products besides cigarettes

Additional Information

Official title Determinants of Multiple Health Risk Behaviors Among Latinos
Principal investigator Larkin L. Strong, PHD
Description Study Participation: If you are eligible and choose to take part in this study, you can choose to visit the clinic 2 times or have research staff visit you in your home or a community setting (such as a church or community center) 2 times. At the first visit (this is the same visit where you complete the in-person screening test): - You will have your height, weight, and waistline measured. - You will be given a smart phone to take home with you. You will answer questions on the smart phone up to 5 times a day for 7 days. The phone will beep at random times (4 times per day) and set times (in the evening) to prompt you to answer questions about what you are doing and your current thoughts and feelings. These questions should take about 5-7 minutes to complete each time. - You will be given an accelerometer (a movement meter). The accelerometer is a small device worn on your hip that measures the amount of physical activity you do. You will wear the accelerometer for 7 days in a row. - You will receive training on how to use the smart phone and the accelerometer. At the second visit, you will return the smart phone and the accelerometer. At both study visits, you will be asked to complete questionnaires that ask about your feelings, moods, and behaviors. You will complete 36 questionnaires at the first visit (a total of 474 questions) and 25 questionnaires at the second visit (a total of 278 questions). These questionnaires should take about 60 to 90 minutes to complete. Throughout the study, you will be contacted by mail, email, or telephone for reminders of visits. You will be reminded before each visit. You will be asked to provide the names and contact information for family and/or friends should the study staff have trouble reaching you. Confidentiality: Each time you complete a survey on the smart phone, your answers will be saved on the phone. When you return the phone, all of your answers will be downloaded from the phone to a secure server, where they will be stored. Then, all of your information will be deleted from the phone. Your name or other personal information will not be stored on the phone. Your name and other identifying information will not be stored together in the same files as other information you provide during your participation in the study. The link between your identifying information and other data will be kept in a separate file and securely protected. The link between you and the study data will be destroyed 5 years after the study ends. Length of Study: You will be considered off study when you complete the second visit. This is an investigational study. Up to 225 participants will take part in this study. All will be enrolled at MD Anderson.
Trial information was received from ClinicalTrials.gov and was last updated in October 2016.
Information provided to ClinicalTrials.gov by M.D. Anderson Cancer Center.