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Spots Global Cancer Trial Database for Perioperative Ostomy Self-Management Telehealth for Cancer Patients and Family Caregivers

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Perioperative Ostomy Self-Management Telehealth for Cancer Patients and Family Caregivers

Official Title: Perioperative Ostomy Self-Management Telehealth (Periop-OSMT) for Cancer Patients and Family Caregivers

Study ID: NCT03970070

Study Description

Brief Summary: This phase II trial studies how well Perioperative Ostomy Self-Management Telehealth (Periop-OSMT) provides patients and their caregivers information about ostomy and ostomy care. Periop-OSMT may help to understand patient preparedness to do ostomy self-care, confidence in doing ostomy self-care, knowledge of ostomy self-care, quality of life, mood, use of medical services, and financial burden.

Detailed Description: PRIMARY OBJECTIVE: I. Assess the feasibility and acceptability of the Periop-OSMT as measured by the percentage of patients and support persons/family caregivers (FCGs) who agree to participate; complete \>= 80% of the intervention; and report satisfaction with the intervention (through structured exit interviews). SECONDARY OBJECTIVES: I. Examine the patterns and trajectories for patient outcomes pre- and post-intervention, including patient activation, self-efficacy, ostomy-related knowledge, health related quality of life (HRQOL), medical care utilization, and financial burden. II. Examine patterns and trajectories for support person/FCG outcomes pre- and post-intervention, including quality of life (QOL). III. Using qualitative methods, evaluate the acceptability of the intervention as reported by participants. OUTLINE: Patients and/or support persons/family caregivers complete Periop-OSMT session in-person or via telephone over 20-40 minutes before surgery and before hospital discharge, and group telehealth session over 1.5-2 hours at weeks 1-3, 4, 5, 6, and 7 post discharge. After completion of study intervention, participants are followed up for 6 months.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Banner University Medical Center - Tucson, Tucson, Arizona, United States

City of Hope Medical Center, Duarte, California, United States

University of Pennsylvania/Abramson Cancer Center, Philadelphia, Pennsylvania, United States

Contact Details

Name: Virginia Sun

Affiliation: City of Hope Comprehensive Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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