Adapting Multiple Behavior Interventions That Effectively Improve Cancer Survivor Health Cancer Survivor Health

Not Applicable

Active, not recruiting

• Conditions: Breast Cancer; Colorectal Cancer; Endometrial Cancer; Kidney Cancer; Multiple Myeloma; Ovary Cancer; Prostate Cancer; Thyroid Cancer; Non-Hodgkin Lymphoma

• Registration Number: NCT04000880
• Lead Sponsor: University of Alabama at Birmingham

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-6-21
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: All
• Target Recruitment: 603

Inclusion Criteria

Inclusion Criteria:<br><br> - Age 50 years or older<br><br> - Resident of the continental United States<br><br> - Diagnosed with multiple myeloma, non-Hodgkin lymphoma, or localized kidney or<br> ovarian cancer; or [localized (includes in situ) through regional] breast,<br> colorectum, endometrium, thyroid, or prostate cancer.<br><br> - Completed primary treatment (surgery, radiation or chemotherapy). Active<br> surveillance among men with prostate cancer or women with ductal carcinoma in situ<br> is acceptable.<br><br> - Completion of the 8th grade of school. Able to read and write English.<br><br> - Normal blood pressure or those with high blood pressure for whom physician<br> permission was granted.<br><br> - Community dwelling.<br><br> - Reside in an area that receives wireless coverage.<br><br> - Have an active email address or be willing to have one created for the study.<br><br> - Current body mass index of greater than or equal to 25 kg/m2, but less than 50<br> kg/m2.<br><br> - Current physical activity level is less than 150 minutes of moderate-to-vigorous<br> exercise per week.<br><br>Exclusion Criteria:<br><br> - Participation in another diet and exercise program.<br><br> - Evidence of progressive cancer of the eligible types.<br><br> - Recurrence of the eligible cancer types (exceptions are biochemical recurrence of<br> prostate cancer).<br><br> - A physician has provided instruction to limit current physical activity.<br><br> - Pre-existing medical conditions that preclude adherence to an unsupervised weight<br> loss intervention (e.g., pregnancy, severe orthopedic conditions, impending hip or<br> knee replacement (within 6 months), end-stage renal disease, paralysis, dementia,<br> blindness, unstable angina, untreated stage 3 hypertension, or recent history of<br> heart attack, congestive heart failure or pulmonary conditions that required oxygen<br> or hospitalization within 6 months).<br><br> - Second primary cancers, with the exception of non-melanoma skin cancer, or if the<br> initial and second cancers are both deemed eligible cancers.<br><br> - Reside in a skilled nursing or assisted living facility.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Change in dietary quality and intake (Patient reported outcome).;Change in dietary quality and intake (Patient reported outcome).;Change in dietary quality and intake (Patient reported outcome).;Change in dietary quality and intake (Patient reported outcome).;Change in dietary quality and intake (Patient reported outcome).;Change in body weight;Change in body weight;Change in body weight;Change in body weight;Change in body weight;Change in physical activity and sleep (Measured by actigraphy);Change in physical activity and sleep (Measured by actigraphy);Change in physical activity and sleep (Measured by actigraphy);Change in physical activity and sleep (Measured by actigraphy);Change in physical activity and sleep (Measured by actigraphy)