A Web-based Tailored Health Behavior Intervention for Breast and Colon Cancer Survivors (eWellness)

Completed · Not applicable

Conditions studied: Nutrition, Physical Activity

In brief

The primary objective of this study is to compare the differences in fruits and vegetable intake and physical activity from pre- to post- study between the intervention and control groups (i.e. the difference in differences). The study involves the use of web-based educational materials over a four week period. The investigators hypothesize that those in the intervention group will show a greater increase in fruit and vegetable intake and engage in more physical activity than those randomized to the control group. Eligible breast and colorectal cancer survivors from the UNC Health Registry/Cancer Survivorship Cohort (UNC HR/CSC) will be selected, consented, and randomized to either the intervention or control group. Both groups will fill out baseline surveys. The intervention group will receive a total to 4 newsletters for 4 weeks and at the beginning of week 5, they will asked to complete the follow-up survey online. The intervention newsletters focus on increasing physical activity and healthy diets. The control group will receive 4 newsletters in the same time frame as the intervention. The focus of the control group's newsletters will be on topics relevant to cancer survivors (e.g. getting back to work after treatment, managing finances) but will not focus on physical activity or diet. All contact with participants will take place online (i.e. surveys and newsletter delivery) from the study web site.

Key facts

Study ID

NCT04188002

Run by

University of North Carolina, Chapel Hill

People needed

49

Starts

2017-03-25

Expected to finish

2018-08-01

Last updated by the study team

2019-12-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• ≥18 years of age
• primary language is English
• histologically confirmed stage 1-111A invasive breast cancer or stage 1-3 colorectal cancer
• between at least 6 months to 5 years since completion of all primary cancer treatments (e.g. surgery, radiation, chemotherapy with the exception of women on adjuvant Herceptin therapy)
• have access to the internet; have an email and/or cell phone (to accept text message reminders from the study).

You may not qualify if…

• Include women that may be pregnant and anyone that is/has:
• A history of another cancer (exception for non-melanoma skin cancers)
• Self-reported comorbidities that would preclude engaging in physical activity safely (e.g. functional limitations or symptomatic cardiovascular or pulmonary disease)
• Plans or scheduled for major surgery (including breast reconstruction) during the intervention time frame
• Any psychiatric illness that would make it difficult to participate in the study

Where it is running

• University of North Carolina at Chapel Hill — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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