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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05745038
Other study ID # UOCPC22065
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 29, 2023
Est. completion date June 30, 2025

Study information

Verified date March 2024
Source University of Rochester
Contact Kah Poh Loh
Phone 585-276-4353
Email Kahpoh_Loh@URMC.Rochester.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if a social network support program (SOcial Networks to Activate Trust & Adherence or SONATA) is helpful for older individuals receiving cancer treatment. The SONATA program will last for about 4 months. There are a total of 6 coaching sessions. The first 5 sessions will be held approximately every 1 to 2 weeks. Session 6 or the final session will be held approximately 1 to 2 months after session 5. Each session will last for about 1 to 2 hours.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date June 30, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Patient Inclusion Criteria: - Age =65 years - A diagnosis of cancer - Planning to initiate or during first three months of oral anticancer treatments - Able to identify at least one network member to participate with them - Able to speak English - Able to provide informed consent Exclusion Criteria: - Any psychiatric or cognitive impairments interfering with participation as determined by the treating oncology team - Enrolled on oral anticancer therapeutic trials Network Members: Inclusion Criteria: 1. Age =18 years 2. Identified as a network member by subjects enrolled on the study (up to 10 network members) 3. Able to speak English. 4. Able to provide informed consent Exclusion Criteria: None

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
SONATA
The SONATA intervention is composed of five components, network diagnostics, network engagement, opportunity creation, skill building and goal-setting, and feedback, that will be audio-recorded and held over six scheduled sessions.

Locations

Country Name City State
United States University of Rochester Rochester New York

Sponsors (1)

Lead Sponsor Collaborator
University of Rochester

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility - SONATA Intervention Number of patients approached who consent 20 Weeks
Primary Acceptability- SONATA Intervention Average general acceptability score using the Theoretical Framework of Acceptability questionnaire. An eight item (range 1 to 5 for each item) psychometrically validated and theoretically informed tool which assesses the following constructs - affective attitude, burden, ethicality, perceived effectiveness, intervention coherence, self-efficacy, opportunity costs, and general acceptability. 20 Weeks
Secondary Estimate - Social Support Assessed using the Medical Outcomes Study Social Support Survey. The Medical Outcomes Study Social Support Survey is a 19-item survey (range 1-5 for each item) to assess four domains of emotional/informational support, instrumental support, positive social interaction, and affection; higher scores indicate greater social support. Subjects will be asked about their perceptions of their own social support. 20 Weeks
Secondary Estimate - Trust in Healthcare Professionals Assessed using the the Human Connection (THC) Scale. The THC scale is A 16-item scale (range 1 to 4 for each item); higher scores indicate greater trust. 20 Weeks
Secondary Estimate - Adherence to oral anticancer treatments Assessed using the Domains of Subjective Extent of Nonadherence (DOSE-Nonadherence). The DOSE-Nonadherence scale is a three-item scale (range from none of the time to every time for each item) with eighteen additional items that assesses reasons for non-adherence. 20 Weeks
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