Using Telehealth to Enhance Oral Health for Cancer Survivors
F.L.O.S.S. Project (Facilitated Lessons on Oral and Systemic Health in Survivors)
This study tests whether using telehealth can help cancer survivors improve their oral health and prevent problems after their treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 25 Years to 75 Years |
| Sex | All |
| Sponsor | Georgetown University Academic / other |
| Locations | 1 site (Washington D.C., District of Columbia) |
| Trial ID | NCT06315855 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of a Telehealth Intervention (THI) aimed at preventing oral complications and improving oral health among cancer survivors. Participants will be randomly assigned to receive either the THI or Usual Care (UC) over a six-month period. The study will assess oral health outcomes, quality of life, and systemic inflammation through intraoral imaging and saliva sample analysis. A total of 100 cancer survivors will be recruited for this study, with a focus on those who are at least six months post-treatment.
Who should consider this trial
Good fit: Ideal candidates are cancer survivors aged 25-75 who are at least six months post-treatment and own a smartphone.
Not a fit: Patients with head and neck/oral cancers or those currently undergoing cancer treatment may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve oral health and quality of life for cancer survivors.
How similar studies have performed: Previous studies have shown promising results using telehealth approaches for managing health conditions, indicating potential success for this intervention.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * male and female cancer survivors who are either ≥ 6 months after competing primary therapy for cancer treatment (N=100) * between 25-75 years of age * all race/ethnic groups * own a smart phone. Exclusion Criteria: * all head and neck/oral cancer survivors * less then 25 years and older than 75 years of age * recurrence/second cancers or undergoing treatment * unable to provide informed consent.
Where this trial is running
Washington D.C., District of Columbia
- Georgetown Lombardi Office of Minority Health — Washington D.C., District of Columbia, United States (Recruiting)
Study contacts
- Study coordinator: Smith
- Email: ds1924@georgetown.edu
- Phone: 202-687-5367
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.