Hypopharynx Cancer, Larynx Cancer, Oral Cavity Cancer, Oropharynx Cancer
Conditions
Brief summary
The purpose of the study is to design a physical activity and dietary intervention for head and neck cancer patients.
Interventions
BEHAVIORALENHANCE Intervention - Exercise and Nutrition
During radiation, participants will attend in-person supervised resistance training sessions once a week for 7 weeks, followed by 2 ZOOM video conference supervised resistance training sessions every week for 5 weeks, after radiation. Sessions will last approximately 30 minutes. During radiation, participants will be provided 15 meals each week for 7 weeks, 105 meals total. Participants will be asked to participate in 1 weekly dietary coaching session (in-person during radiation and video conference following radiation), create weekly SMART goals, follow an alternative Mediterranean diet pattern, and log all meals, snacks, and supplements consumed for the 12-week intervention.
BEHAVIORALENHANCE Intervention - Nutrition Only
During chemoradiotherapy, participants will be provided 15 meals each week for 7 weeks (105 meals total) that will accommodate common NIS concerns (ex. dysphagia and difficulty chewing) following an aMED dietary pattern (5 breakfast, 5 lunch, and 5 dinner), will be taught proper portion size, and will be asked to record percentages of each meal consumed in a provided food journal, in addition to any outside meals, snacks, or nutritional supplements. They will be provided with dietary coaching weekly to discuss NIS, aMED diet compliance, and set weekly SMART goals (approximately 30 min). Following completion of chemoradiotherapy (5 weeks), participants will be provided dietary coaching weekly (in-person or via videoconference), discuss NIS, aMED diet compliance at home, and set weekly SMART goals (30 min). Trainers will monitor participants' Fitbit active minutes in real time throughout the intervention period and provide aerobic exercise encouragement accordingly.
Sponsors
H. Lee Moffitt Cancer Center and Research Institute
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* \>18 years old * Newly diagnosed tumors of the oral cavity, oropharynx, hypopharynx, or larynx * No documented or observable psychiatric or neurological disorders that would interfere with study participation (e.g., dementia, psychosis) * Able to speak and read English * Able to consume food orally * Willing to consume an alternative Mediterranean diet * Scheduled to receive treatment with radiation or chemoradiation * Screened via the Physical Activity Readiness Questionnaire (PAR-Q+) with medical clearance of treating physicians, as necessary * Able to provide informed consent
Exclusion criteria
* Women who are pregnant * Head and Neck Cancer not the primary diagnosis * Patients scheduled to receive surgery * Patients on enteral or parental nutrition
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants Recruited - Feasibility | 12 Months | The study will be deemed feasible if ≥ 60% of eligible participants are enrolled |
| Number of Participants who Complete Questionnaire - Retention - Feasibility | 12 weeks | The study will be deemed feasible if ≥ 70% of participants complete post intervention questionnaire. |
| Participant Satisfaction of Timeline - Feasibility | 12 weeks | The study will be deemed feasible if ≥ 70% of participants like the timing of the intervention using a likert scale (scale range Strongly agree to Strongly disagree) |
| Participant Average Attendance - Assessment Completion - Adherence | 12 weeks | Participant assessment completion will be deemed successful if participant average attendance is ≥10 weeks of sessions (out of 12) |
| Number of Participants who Complete Task/Goals - Adherence | 12 weeks | Study adherence will be deemed successful if ≥70% of participants report weekly tasks/goals adherence (e.g., gym and diet) |
| Participant Satisfaction Assessed with 5 Point Scale - Acceptability | 12 weeks | Participants satisfaction will be measured using a 5 point scale (1 is the lowest, 5 is the highest) exit survey administered at the post-intervention follow-up. |
| Participant Intent to Continue Assessed with 5 Point Scale - Acceptability | 12 weeks | Participants intent to continue will be measured using a 5 point scale (1 is the lowest, 5 is the highest) exit survey administered at the post-intervention follow-up. |
| Participant Knowledge Gained Assessed with 5 Point Scale - Acceptability | 12 weeks | Participants knowledge gained will be measured using a 5 point scale (1 is the lowest, 5 is the highest) exit survey administered at the post-intervention follow-up. |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORSylvia Crowder, PhD
Moffitt Cancer Center
Outcome results
None listed