Viewing Study NCT04630015



Ignite Creation Date: 2024-05-06 @ 3:27 PM
Last Modification Date: 2024-10-26 @ 1:49 PM
Study NCT ID: NCT04630015
Status: COMPLETED
Last Update Posted: 2023-05-09
First Post: 2020-11-13

Brief Title: Expanded Evaluation of the Survivorship Wellness Group Program in the Context of COVID-19 and Telehealth
Sponsor: University of California San Francisco
Organization: University of California San Francisco

Study Overview

Official Title: Expanded Evaluation of the Survivorship Wellness Group Program in the Context of COVID-19 and Telehealth
Status: COMPLETED
Status Verified Date: 2023-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study evaluates the effects of the Survivorship Wellness Group Program following active treatment as well as to learn from Survivorship Wellness participants about their concerns regarding the current COVID-19 pandemic This study may help to evaluate the impact of the survivorship program on patient well-being provide evidence for use in grant application and publications and ultimately inform the continued improvement of survivorship care
Detailed Description: PRIMARY OBJECTIVES

1 To examine the feasibility and acceptability of implementing an interdisciplinary goal-setting clinical group program focused on domains of physical psychological and spiritual wellness for survivors of cancer at University of California San Francisco UCSF
2 To determine preliminary efficacy of the Survivorship Wellness intervention in regards to

1 Increasing knowledge of and perceived confidence in execution of health behavior changes in domains of physical emotional and spiritual wellness for survivors of cancer
2 Increasing quality of life
3 Reducing symptoms of depression and anxiety
4 Increasing physical activity
3 To assess differences in patient wellbeing and in the impact of the Survivorship Wellness program during the period of COVID-19 and telehealth classes

OUTLINE

Patients complete surveys over 5-10 minutes at baseline ie before participating in the program and at 9 and 15 weeks follow up on the impact of COVID-19 on survivorship Patients also complete a survey assessing how patients rate telehealth classes in the Survivorship Wellness program

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
NCI-2020-08530 REGISTRY NCI Clinical Trials Reporting Program CTRP None