Web-based psychosocial screening for head and neck cancer patients
Northern Alberta Psychosocial Telecare (NAPT) Screening for Surgical Head and Neck Cancer Patients: a Randomized Controlled Trial
This study is testing a new online tool to see if it can help head and neck cancer patients manage their mood and stress better than regular care after surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Alberta Academic / other |
| Drugs / interventions | chemotherapy, radiation |
| Locations | 1 site (Edmonton, Alberta) |
| Trial ID | NCT03215199 on ClinicalTrials.gov |
What this trial studies
This clinical trial compares a web-based psychosocial screening application to standard care for patients who have undergone surgery for head and neck cancer. The NAPT App will monitor patients' mood and distress levels using validated scoring systems, allowing for timely referrals to mental health services if needed. Assessments will occur at baseline, two weeks post-surgery, and monthly for up to 12 months, with a focus on various health outcomes including treatment adherence and quality of life. The primary goal is to evaluate the effectiveness of the application in reducing cancer-related distress over six months.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are newly diagnosed with non-recurrent head and neck cancer and have undergone primary surgical treatment.
Not a fit: Patients with a history of psychiatric illness, recurrent head and neck cancer, or those who have previously received chemotherapy or radiation therapy may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve mental health support for head and neck cancer patients, leading to better overall outcomes.
How similar studies have performed: Other studies have shown success with web-based psychosocial interventions, indicating potential for this approach to be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years * New (non-recurrent) head and neck cancer * Primary surgical treatment Exclusion Criteria: * \<18 years * Recurrent head and neck cancer * Previous chemotherapy or radiation therapy * History of psychiatric or psychologic illness * History of previous cancers or cancer distress
Where this trial is running
Edmonton, Alberta
- University of Alberta — Edmonton, Alberta, Canada (Recruiting)
Study contacts
- Study coordinator: Brittany Barber
- Email: brittanybarber0@gmail.com
- Phone: 6464459592
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.