Viewing Study NCT04714164



Ignite Creation Date: 2024-05-06 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 1:54 PM
Study NCT ID: NCT04714164
Status: TERMINATED
Last Update Posted: 2024-01-05
First Post: 2021-01-07

Brief Title: Cognitive Behavioral Therapy Group for Older Adults Delivered by Telethealth
Sponsor: Nova Scotia Health Authority
Organization: Nova Scotia Health Authority

Study Overview

Official Title: Feasibility of Delivering Group Cognitive Behavioral Therapy for Older Adults With Depression and Anxiety by Telehealth
Status: TERMINATED
Status Verified Date: 2024-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: We had difficulty with participation in the study for our initial Zoom CBT group
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The present aim of the study is to to adapt an established manualized enhanced Group CBT CBT-E for seniors to a telehealth format which will allow us to offer the group virtually during the COVID-19 pandemic
Detailed Description: The goal of this project is to adapt an established manualized enhanced Group CBT CBT-E for seniors to a telemedicine format Currently the Geriatric Psychiatry service associated with the Nova Scotia Health Authority offer two CBT-E groups every year They are usually facilitated by psychiatry residents under the supervision of a staff psychiatrist Due to the risk of COVID-19 we will not be holding in-person groups this year Instead we will offer the group in a smaller telemedicine format For this project we will change the group structure and activities to allow its delivery in a virtual format This study will assess feasibility tolerability of the telehealth format by using the System Usability Scale and Group Satisfaction Survey It will also assess response to online therapy buy using pre- and post-group questionnaires including the Beck Depression Inventory Beck Anxiety Inventory and Perceived Quality of Life Questionnaire Paired t-tests will be used to analyse the data and determine whether there has been an improvement in participants symptoms and quality of life

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