Impact of Expiratory Muscle Strength Training (EMST) on Swallowing Function in Persons Undergoing Radiotherapy With or Without Chemotherapy (CRT) for Cancers of the Head and Neck (HNCA)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Head and Neck Neoplasms
- Sponsor
- University of Wisconsin, Milwaukee
- Enrollment
- 30
- Locations
- 2
- Primary Endpoint
- Feeding-tube-free food intake (days)
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
This study is a randomized trial examining the impact of expiratory muscle strength training (EMST) on maintenance of safe and efficient oropharyngeal swallow function in persons with cancer of the head and neck (HNCA) undergoing treatment with radiation therapy or chemoradiotherapy (RT/CRT).
Detailed Description
Thirty (30) persons with newly-diagnosed HNCA who will be treated with RT/CRT will be randomized to an 8-week program of either Active Expiratory Muscle Strength Training (EMST) + Standard Care or Sham EMST + Standard Care in order to examine the impact of EMST on swallowing function. The training program will consist of 5 sets of 5 breaths, 5 days per week for 8 weeks, coincident with RT/CRT. Patients randomized to the Active EMST group will use the EMST150 (product name) expiratory muscle strength trainer according to package instructions. Those randomized to the Sham EMST group will use an EMST150 device that has been modified to eliminate resistance to airflow. All subjects will be evaluated prior to initiation of cancer treatment (baseline assessment), 4 weeks into cancer treatment and again at the completion of cancer treatment (8 weeks after initiation of treatment). Assessment will include measurement of maximum expiratory pressure (MEP), a videofluoroscopic swallow study (VFSS) to objectively document swallow function, and administration of swallow-related quality of life (QOL) questionnaires.
Investigators
Barbara Pauloski
Associate Professor
University of Wisconsin, Milwaukee
Eligibility Criteria
Inclusion Criteria
- •New diagnosis of cancer in the oral cavity, oropharynx, hypopharynx, or larynx;
- •Planned treatment with primary radiotherapy with or without chemotherapy;
- •Age 18 or older and able to provide consent;
- •Ability to use the EMST150 device (hold in mouth and maintain lip seal)
Exclusion Criteria
- •Primary surgery to the head and neck (neck dissection is permitted);
- •Unknown primary tumor;
- •Primary cancers of the nasopharynx, paranasal sinuses, salivary glands and skin.
- •Progressive neurologic condition affecting muscle strength (e.g. amyotrophic lateral sclerosis (ALS), Parkinson's disease)
- •Dysphagia not related to HNCA (e.g. unresolved swallowing difficulty post-stroke or post--traumatic brain injury (TBI))
- •Prior history of head and neck radiotherapy
Outcomes
Primary Outcomes
Feeding-tube-free food intake (days)
Time Frame: 8 weeks
the number of days from the beginning of the study until change in feeding status from 100% oral intake to combined oral intake and tube intake and/or 100% tube feeding will be calculated
Secondary Outcomes
- Presence of pharyngeal residue (dichotomous)(8 weeks)
- Penetration-Aspiration Scale rating (number)(8 weeks)
- Timing of Aspiration (category)(8 weeks)
- Extent of hyoid movement (mm)(8 weeks)
- Upper esophageal sphincter (UES) opening width (mm)(8 weeks)