Enhance Wellness for Individuals With Long-Term Physical Disabilities

Multiple Sclerosis Clinical Trial

Official title:

Project Enhance for Adults Aging With Long-Term Physical Disability

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02815878
• Other study ID #: 47035
• Status: Completed
• Phase: N/A
• First received: June 22, 2016
• Last updated: March 30, 2018
• Start date: May 12, 2014
• Est. completion date: November 2017

Study information

• Verified date: October 2017
• Source: University of Washington
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This project is an adaptation trial, testing the efficacy of an evidence-based community wellness program, Enhance Wellness (http://www.projectenhance.org/enhancewellness.aspx), in a sample of middle and older-aged adults living with multiple sclerosis, spinal cord injury, post-polio syndrome and muscular dystrophy.

Description:

This is a quasi-experimental project, comparing the effects of Enhance Wellness in a sample of adults aged 45 years or older and living with long-term physical disability, to two quasi-control groups: a sample of adults without long-term disability participating in Enhance Wellness, and a sample of adults with long-term disability not participating in Enhance Wellness. Outcomes are collected pre-intervention and post-intervention, approximately 6-months apart.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 240
• Est. completion date: November 2017
• Est. primary completion date: November 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 45 Years and older

Eligibility

Inclusion Criteria:

• Multiple Sclerosis, Muscular Dystrophy, Post-Polio Syndrome, or Spinal Cord Injury diagnosis (Group 1 and 3)

• Living in King County, Washington (Group 1 only)

• Ability to read and understand English

Exclusion Criteria:

• Active suicidal ideation

• Requires the use of a mechanical ventilator to breathe or speak

Related Conditions & MeSH terms

• Multiple Sclerosis
• Muscular Dystrophies
• Muscular Dystrophy
• Post-polio Syndrome
• Postpoliomyelitis Syndrome
• Spinal Cord Injuries
• Spinal Cord Injury

Intervention

Behavioral:
• Enhance Wellness
A 6-month health promotion intervention which pairs participants with a wellness coach to identify and pursue a health-related goal of their choosing.

Locations

Country	Name	City	State
United States	University of Washington	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Questionnaire: Level of reported self-efficacy as measured by the University of Washington Self-Efficacy Scale Questionnaire	This is a self-reported measure of perceived efficacy to manage conditions or symptoms related to a person's physical disability or condition. Greater scores represent greater self-efficacy.	6-months
Primary	Questionnaire: Patient Reported Outcome Measurement Information System (PROMIS) Pain Interference Short Form	Self-reported measure of pain interference. Greater score indicate greater pain interference.	6-months
Primary	Questionnaire: Patient Reported Outcome Measurement Information System (PROMIS) Depression Short Form	Self-reported measure of depression. Greater scores indicated greater depressive symptoms.	6-months