Feasibility of Early Swallowing and Speech Intervention for Head and Neck Cancer Patients Treated SURGically (NCT06192771)
๐ฉบ Plain-English Summary (8th-Grade Level)
Oral cavity cancer (OCC) is one of the most common cancers worldwide, with tongue cancer being one of the most common subtypes. Patients with oral cancers can experience painful swallowing, swallowing difficulty (dysphagia), and associated weight loss long after surgery. Not only is dysphagia an independent predictor of quality of life (QoL) in cancer survivorship, it can also have a devastating impact on the health of patients resulting from complications such as pneumonia, malnutrition and feeding tube dependence. Emerging evidence suggests that patients undergoing surgery benefit from engaging with speech-language pathologists (SLPs) before problems arise, to learn swallow strategies that may become useful in their rehabilitation. This in turn has the potential to reduce complications and minimize the length of feeding tube dependency. This study will assess the feasibility of conducting a prospective clinical trial that would evaluate the effects on patient health, function and overall benefit of early and systematic SLP speech and swallowing intervention for head and neck cancer patients planned for curative surgical treatment. We will also assess long-term changes in select clinical and patient-reported outcomes comparing their status before, and one month after, treatment.
Who can join: Review the eligibility criteria below.
Location: University Health Network โ Toronto, Ontario
Age range: 18 Years
๐งช Interventions in This Study
- ESSI-SURG (BEHAVIORAL)
- Standard-of-Care (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- University Health Network โ Toronto, Ontario
๐ Contact the Study Coordinator
Phone: (416) 946-3826
Email: trixie.reichardt@uhnresearch.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Dysphagia
- Optimizing Dysphagia Treatment Delivery in Acute Care: A Hybrid Efficacy Implementation Trial โ Nashville, Tennessee
- Standardizing Swallow Pressure Measurements โ Madison, Wisconsin
- Aspiration in Acute Respiratory Failure Survivors 2 โ Stanford, California
- Non-standardized vs. Standardized Screening for Dysphagia โ Miami, Florida
- A Digital Therapeutic Platform for Swallowing and Drooling Problems in Parkinson's โ Evanston, Illinois
Explore by condition: All Dysphagia clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.