Head and Neck Cancer, Oropharynx Cancer
Conditions
Keywords
Prophylactic Swallowing Therapy
Brief summary
Clinician directed prophylactic swallowing therapy will improve immediate (four weeks +/- two weeks) and short-term (26 weeks +/- four weeks) post-treatment swallowing function and quality of life versus patient directed home exercises. The purpose of this prospective, interventional, pilot investigation is to determine whether clinician directed swallowing therapy will improve patient swallowing function outcomes and quality of life in the immediate and short-term basis compared to patients receiving standard of care patient directed independent home swallowing therapy. Patient compliance with home exercises programs is reportedly inconsistent. Patients may experience changes in their physical functioning and overall well-being that may impact their ability to follow-through with independent home therapy. Clinician directed swallowing therapy allows for ongoing assessment of changes that may warrant modifying the therapy program in terms of intensity of exercises and/or expectations. This facilitates individualizing the patient's therapy plan to maximize their function and ability to achieve goals. It is anticipated that individualizing swallowing therapy through weekly session will result in improved swallowing function.
Detailed description
This is a single-site, two-arm, 1:1 randomized, prospective, interventional, pilot study to determine whether clinician directed swallowing therapy will improve patient swallowing function outcomes when compared to patient-directed home-based swallowing therapy. The investigators anticipate at least 40 subjects will need to be enrolled/consented in order to obtain the accrual goal of 15 evaluable subjects for each group for a total of 30 participants. All subjects in each group will receive a face-to-face education session with a speech pathologist to review a recommended program of swallowing exercises prior to initiation of chemoradiation at their baseline (pre-treatment evaluation session).
Interventions
OTHERProphylactic Swallowing Home Exercise Program
The home exercise program will consist of six exercises that are recommended to be practiced three times per day. Subjects will complete a weekly exercise log to track compliance.
OTHERClinician-Directed Prophylactic Swallowing Exercises
Once weekly face-to-face meetings with a study speech pathologist for a total of six sessions, to participate in active swallowing exercises
Sponsors
University of Miami
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
1. Diagnosis of head and neck cancer (sites: oropharynx: human papillomavirus (HPV) related and non HPV related tonsil and base of tongue) 2. Scheduled to undergo definitive chemoradiation therapy 3. At least 18 years of age or older 4. Subject must have the ability to understand and the willingness to sign a written informed consent document.
Exclusion criteria
1. Surgical management in addition to chemoradiation therapy; 2. Cancer of the sinus, brain, or parotid; 3. Prior treatment for head and neck cancer; 4. Receiving chemoradiation treatment at an outside institution (i.e., non-University of Miami (UM) clinic); 5. Prior history of dysphagia unrelated to the current diagnosis of head and neck cancer; 6. Prior neurologic disorder (i.e., Cerebrovascular accident (CVA), Traumatic brain injury (TBI), dementia) or current degenerative neuromuscular disease; 7. History of prior c-spine surgery; 8. History of prior vocal fold immobility
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in swallowing status | Baseline, Up to 6 weeks | Swallowing status will be measured using Functional Oral Intake Scale (FOIS). FOIS has a range from 0 (most restrictive) to 7 (least restrictive). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in quality of life as measured by PSS-HN | Baseline to 6 weeks, Baseline to 30 weeks | Performance Status Scale - Head and Neck (PSS-HSN) is a questionnaire with a total score ranging from 100 (normal function) to 0 (limited function). |
| Change in quality of life as measured by EAT-10 | Baseline to 6 weeks, Baseline to 30 weeks | Eating Assessment Tool-10 (EAT-10) is a questionnaire with a total score ranging from 0 to 40 with the lower score indicating better function. |
| Change in swallowing status as measured by FOIS | Baseline, Up to 30 weeks | FOIS has a range from 0 (most restrictive) to 7 (least restrictive). |
| Proportion of patients requiring further swallowing therapy | Baseline to 6 weeks, Baseline to 30 weeks | Proportion of patients requiring further swallowing therapy post study intervention as per treating physician discretion |
| Change in Pharyngeal Swallowing Efficiency and Safety as measured by DIGEST Safety Grade | Baseline to 6 weeks, Baseline to 30 weeks | DIGEST is a measure of pharyngeal swallowing efficiency and safety. The DIGEST measure incorporates 2 measures: 1. Safety as determined by the Penetration Aspiration Scale with a score ranging from 0 (safe) to 4 (life-threatening unsafe); and 2. Efficiency as determined by the quantity of residue observed on the videoflouroscopic swallowing study with a score ranging from 0 (efficient) to 4 (life-threatening inefficiency). These two measures combine for an overall score, ranging from 0 (no pharyngeal dysphagia) to 4 (life-threatening dysphagia). |
| Change in quality of life as measured by UW-QOL | Baseline to 6 weeks, Baseline to 30 weeks | University of Washington Quality of Life (UW-QOL) is a questionnaire with a total score ranging from 0 to 100 with the higher score indicating poorer health outcomes. |
Countries
United States
Outcome results
None listed