NCT04617678Active, not recruiting
A Comprehensive Approach to Head and Neck Cancer Prehabilitation
Source: ClinicalTrials.gov · Last updated 16 Jan 2026
Brief summary (registry, in English)
Head and neck cancer accounts for 3% of malignancies in the United States. However, the diagnosis and treatment for head and neck cancer is considered to be debilitating. Not because of its morbidity, but due to the extremely rigorous treatment course which has a profound impact on patients physical, social, and emotional functioning. Disfigurement and sensorimotor deficits further compound this impact. Head and neck cancer patients contend with treatments that can significantly affect their quality of life. Treatment regularly results in decreased functional capacity and decreased quality of life. Physical impairments are manifested through, but not limited to, disfigurement, deconditioning, communication issues, "swallowing, speech, breathing, and cancer-related fatigue". Premorbid factors such as preexisting anxiety and depression, chemical dependency, financial barriers, and lack of social support system are unique obstacles to the head and neck cancer population impacting treatment and outcomes. Due to these factors, patients experience higher rates of anxiety and depression, psychological distress, and fear of cancer recurrence. In fact, "compared with other survivors of cancer, head and neck cancer survivors are almost 2 times more likely to die from suicide". In view of the aforementioned research, Roger Maris Cancer Center's head and neck cancer will implement a prehabilitation program that evaluates each patient using standardized screening tools and provide personalized education and interventions. This project evaluates a more comprehensive and proactive multidisciplinary approach to improve treatment and outcomes in head and neck cancer patients.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 23 Oct 2020
- Start date
- 21 Oct 2021
- Primary completion date
- 5 Dec 2025
- Lead sponsor
- Sanford Health
- Diseases
- Head and neck cancer
- NCT number
- NCT04617678
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 21 Oct 2021 to the primary completion date, 5 Dec 2025
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Patients with cardiac arrhythmia with implanted pacemaker
- Patient has a metal allergy
Other
- Patients with other implanted electronic equipment/device
- Patients undergoing external defibrillation
- Pregnant women (per BIS instructions for use, pregnant women should not participate)
- Patient weight exceeding 375 lbs.
Who the study is looking for
- Equal to or greater than 18 years of age
- Diagnosis of head and neck cancer
- Actively pursuing cancer treatment with a curative intent
- Willing and able to provide written consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Sanford Health Coordinator of this site? Confirm its status | Fargo | United States | Unknown status |
| Sanford Health Coordinator of this site? Confirm its status | Sioux Falls | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.