SMLI With Hispanic Cancer Survivors and Caregivers

In the proposed randomized controlled trial, the investigators will test the 12-week SMLI against an attention control condition in 107 dyads of Hispanic cancer survivors who have completed curative treatments within the past two years and their informal caregivers. A 12-week follow-up will determine the sustainability of the intervention. The primary outcome of this trial, vegetable and fruit intake in survivors (secondary in caregivers), will be measured at baseline, 13, and 25 weeks, using validated methods. Additional secondary and exploratory outcomes will add to the rigor of the trial and provide robust findings for future dissemination efforts.

Specific Aim #1: Test the efficacy of the SMLI as compared to attention control among Hispanic female cancer survivors and their caregivers with respect to:

• Increase in fruit and vegetable consumption (measured via self-reported 24-hour recall and objectively with carotenoid skin colorimetry)
• Increase in physical activity (Metabolic Equivalents hours/week of moderate to vigorous physical activity measured by actigraphy) and decrease in symptom severity index

Specific Aim #2: Determine the extent to which improvements in primary and secondary outcomes over weeks 13 and 25 are mediated by social support and self-efficacy.

Inclusion criteria

for female Hispanic cancer survivors:

• 18 years of age or older;
• have access to a telephone,
• speak and understand English or Spanish;
• have finished curative intent treatment for cancer within the previous 10 years and do not have any subsequent cancer treatments planned, except for non-curative intent maintenance therapy, such as hormonal therapy;
• must have at least 1 of the 5 most common cancer-related symptoms (pain, sleep disturbance, anxiety, depression and/or fatigue) with a severity score of 4 or higher on a 0-10 rating scale (based on NCCN guidelines for symptom monitoring and management used successfully in past work); and
• has a caregiver willing to participate in the study with them.

Inclusion criteria

for the caregivers (nominated by the survivor) are:

• age 18 or older;
• able to speak and understand English or Spanish;
• access to a telephone; and
• not currently treated for cancer preserving the distinction between survivor and caregiver. The caregiver can be of any race or ethnicity and any gender.

Exclusion criteria

for survivors:

• Under the age of 18 years
• Does not have access to a telephone
• Completed treatment for cancer more than 1 year ago
• Currently receiving counseling or treatment for special diet or weight loss
• Does not have a caregiver willing to participate with them

Exclusion criteria

for caregivers:

• Under the age of 18 years
• Does not have access to a telephone
• Currently receiving counseling or treatment for special diet or weight loss
• Currently being treated for cancer