Meeting an Unmet Need in Multiple Sclerosis

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

The primary objectives of this study is to examine the efficacy of the Unified Protocol in decreasing depression and anxiety among individuals with MS and the secondary outcomes (e.g., improved well-being, QOL, coping, etc.) that may occur in tandem. To achieve this, the investigation has the following specific aims: Specific Aim 1: Conduct a pilot Randomized Controlled Trial (RCT) of the Unified Protocol among individuals with MS to determine the effectiveness of the intervention in reducing depression and anxiety. Hypothesis 1: Individuals who participate in the Unified Protocol intervention will report a decrease in their depression and anxiety compared to individuals in the control group. Specific Aim 2: Conduct a pilot RCT of the Unified Protocol among individuals with MS to determine the effectiveness of the intervention in improving secondary outcomes of psychological well-being, QOL, coping, and MS symptomatology over time. Hypothesis 2: Individuals who participate in the Unified Protocol intervention will report an increase in psychological well-being, QOL, coping, and MS symptomatology over time compared to participants in the control group. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05953519
Study type	Interventional
Source	Kessler Foundation
Contact	Belinda L Washington, BA
Phone	973-324-8446
Email	bwashington@kesslerfoundation.org
Status	Recruiting
Phase	N/A
Start date	April 10, 2023
Completion date	April 30, 2026

View Details

See also
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