Internet-Based Nutrition Education Program in Preventing Cancer in Participants of Health Maintenance Organizations
This trial is active, not recruiting.
|Condition||unspecified adult solid tumor, protocol specific|
|Treatments||behavioral dietary intervention, dietary intervention, educational intervention, internet-based intervention, preventative dietary intervention, evaluation of cancer risk factors|
|Sponsor||Josephine Ford Cancer Center at Henry Ford Hospital|
|Collaborator||National Cancer Institute (NCI)|
|Start date||August 2005|
|End date||June 2007|
|Trial size||2619 participants|
|Trial identifier||NCT00169312, CDR0000514226, HFH-B40389|
RATIONALE: Websites for nutrition education may be an effective method to help people eat more fruits and vegetables which may lower their risk of cancer.
PURPOSE: This randomized trial is studying how well an internet-based nutrition education program works in preventing cancer in participants of health maintenance organizations.
|United States||No locations recruiting|
|Other Countries||No locations recruiting|
|Denver, CO||Kaiser Permanente - Colorado||no longer recruiting|
|Atlanta, GA||Kaiser Permanente, Georgia||no longer recruiting|
|Minneapolis, MN||HealthPartners Research Foundation||no longer recruiting|
|Seattle, WA||Group Health Cooperative||no longer recruiting|
Change in the number of daily fruit and vegetable servings consumed from baseline to 12 months post intervention
Change in the number of daily fruit and vegetable servings consumed at the 3- and 6-month post-intervention assessments
Proportion of participants who achieve an intake of 5 or more daily fruit and vegetable servings by 12 months
Male or female participants from 21 years up to 65 years old.
DISEASE CHARACTERISTICS: - Current member of any of the following participating health maintenance organizations: - Group Health Cooperative - Kaiser Permanente, Colorado - Kaiser Permanante, Georgia - HealthPartners Research Foundation - Henry Ford Health System/Health Alliance Plan - Must complete a web-based health survey prior to randomization PATIENT CHARACTERISTICS: - No medical or mental health condition that would be adversely affected by increased vegetable and fruit intake - One participant allowed per household PRIOR CONCURRENT THERAPY: - No concurrent anticoagulation therapy (e.g., warfarin) - No other concurrent medications that would be adversely affected by increased vegetable and fruit intake - No grapefruit concurrently with any of the following medications: - Statin for high cholesterol - Blood pressure medications (e.g., Losartan) - Calcium channel blockers - Certain psychiatric medications (e.g., buspirone hydrochloride, triazolam [Halcion], carbamazepine, diazepam [Valium], or midazolam hydrochloride) - Immune suppressants (e.g., cyclosporine or tacrolimus) - Impotence medications (e.g., sildenafil [Viagra]) - Methadone
|Official title||The HMO Cancer Research Network (CRN) - Making Effective Nutritional Choices for Cancer Prevention: The MENU Study|
|Principal investigator||Christine Cole Johnson, PhD|
|Description||OBJECTIVES: Primary - Compare the effects of internet-based nutrition education through untailored websites vs tailored websites (TW) vs TW and tailored human online behavioral interaction (HOBI) on the change in the number of daily fruit and vegetable servings consumed in participants of health maintenance organizations. Secondary - Compare the proportion of participants reporting consumption of 5 or more servings of fruits and vegetables per day at each 3-month interval. - Compare the change in fruit and vegetable servings consumed from baseline to each intermediate time point. - Compare the effects of intervention and observation time in these participants. - Determine the effect of HOBI in these participants. - Compare the impact of participant characteristics, in terms of the effect of the intervention on the change in fruit and vegetable intake, in these participants. OUTLINE: This is a randomized, controlled, single-blind, multicenter study. Participants are stratified according to participating site, gender, and the participant's stage of change readiness. Participants are randomized to 1 of 3 intervention arms. - Arm I (untailored websites): Participants are given unlimited access to an internet-based nutrition education program for up to 6 months. They are provided with 4 serial educational websites at 1, 3, 13, and 15 weeks after initial login. These internet sites provide general information about fruits and vegetables, new recipes with emphasis on fruits and vegetables, and how participants can incorporate them into their diet. Participants complete an online survey at 3 months. - Arm II (tailored websites): Participants are given unlimited access to an internet-based nutrition education program for up to 6 months. They are provided with 4 serial educational websites, at the same timepoints as in arm I, with emphasis on vegetable consumption in weeks 1 and 13 and fruit consumption in weeks 3 and 15. Materials in these websites, including new recipes with emphasis on fruits and vegetables, are tailored and then revised (or retailored) based on individual health-risk information obtained at baseline and at the 3-month online survey. - Arm III (tailored websites and human online behavioral interaction [HOBI]): Participants are given unlimited access to an internet-based nutrition education program for up to 6 months. Participants are provided with 4 serial educational websites with tailored materials as in arm II. They also receive HOBI (tailored e-mail messages) developed and then revised based on health-risk information obtained at baseline and the 3-month online survey. In all arms, participants complete online surveys at 3, 6, and 12 months to measure fruit and vegetable intake and change in long-term risk behavior. For each survey, participants receive up to 6 automatically generated reminder e-mails and 1 mailed announcement. PROJECTED ACCRUAL: A total of 2,619 participants were accrued for this study.|
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