Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
42

Summary

Conditions
Insomnia
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Investigator, Outcomes Assessor)Primary Purpose: Supportive Care

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

PRIMARY OBJECTIVE: To compare the effects of partnered YOCAS, non-partnered YOCAS interventions, and standard care on changes in insomnia measured via Insomnia Severity Index (ISI) among cancer survivors and caregivers SECONDARY OBJECTIVE: To compare the effects of partnered YOCAS, non-partnered YOC...

PRIMARY OBJECTIVE: To compare the effects of partnered YOCAS, non-partnered YOCAS interventions, and standard care on changes in insomnia measured via Insomnia Severity Index (ISI) among cancer survivors and caregivers SECONDARY OBJECTIVE: To compare the effects of partnered YOCAS, non-partnered YOCAS interventions, and standard care on changes in sleep quality measured via Pittsburgh Sleep Quality Index (PSQI) among cancer survivors and caregivers OUTLINE: Cancer survivor-caregiver dyads are randomized to 1 of 3 arms. ARM I: Standard Care: Cancer survivor-caregiver dyads receive their standard care ARM II: Partnered YOCAS: Cancer survivor-caregiver dyads participate in 8 virtual Zoom YOCAS sessions (75 minutes/session, 2 times a week for 4 weeks) together ARM III: Non-partnered YOCAS: Cancer survivors participate in 8 virtual Zoom YOCAS sessions (75 minutes/session, 2 times a week for 4 weeks) alone; caregivers do not receive Zoom YOCAS sessions

Tracking Information

NCT #
NCT04458194
Collaborators
Bassett Medical Center
Investigators
Principal Investigator: Karen Mustian, PhD, MPH University of Rochester