A program to support older cancer patients through social networks
A Single Arm Pilot Trial of a Social Network Intervention (SONATA) for Older Patients With Cancer
This study is testing a new support program that helps older cancer patients connect with others during their treatment to see if they find it helpful and if they stick with it.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 330 (estimated) |
| Ages | 60 Years and up |
| Sex | All |
| Sponsor | University of Rochester Academic / other |
| Locations | 1 site (Rochester, New York) |
| Trial ID | NCT05745038 on ClinicalTrials.gov |
What this trial studies
This pilot study evaluates the feasibility and acceptability of the SONATA program, a social network support intervention designed for older individuals undergoing treatment for advanced cancer. The program consists of six coaching sessions over approximately four months, with the first five sessions occurring every one to two weeks and the final session held one to two months later. The study aims to determine if at least 70% of enrolled patients complete three sessions and if the average acceptability score meets or exceeds four on a five-point scale.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 60 and older with a diagnosis of advanced or likely incurable cancer who can communicate in English.
Not a fit: Patients with psychiatric or cognitive impairments that interfere with participation may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could enhance the support and adherence to treatment for older cancer patients, potentially improving their overall outcomes.
How similar studies have performed: While this approach is relatively novel, similar interventions in geriatric oncology have shown promise in enhancing patient support and adherence.
Eligibility criteria
Show full inclusion / exclusion criteria
Patient Inclusion Criteria: 1. Age ≥60 years 2. A diagnosis of advanced or likely incurable cancer, as determined by the primary oncologist 3. Able to speak English 4. Able to provide informed consent Exclusion Criteria: 1\) Any psychiatric or cognitive impairments interfering with participation as determined by the primary oncology team Network Members: Inclusion Criteria: 1. Age ≥18 years 2. Identified as a network member by patient subjects (up to 10 network members) 3. Able to speak English 4. Able to provide informed consent. Exclusion Criteria: None
Where this trial is running
Rochester, New York
- University of Rochester — Rochester, New York, United States (Recruiting)
Study contacts
- Principal investigator: Kah Poh Loh — University of Rochester
- Study coordinator: Kah Poh Loh
- Email: Kahpoh_Loh@URMC.Rochester.edu
- Phone: 585-276-4353
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.