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NCT Number: NCT02815878

Enhance Wellness for Individuals With Long-Term Physical Disabilities

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.

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Key information

Conditions

Multiple Sclerosis Autoimmune Diseases Autoimmune Diseases of the Nervous System Central Nervous System Diseases Central Nervous System Infections Congenital, Hereditary, and Neonatal Diseases and Abnormalities Demyelinating Autoimmune Diseases, CNS Demyelinating Diseases Enterovirus Infections Genetic Diseases, Inborn Immune System Diseases Infections Muscular Diseases Muscular Disorders, Atrophic Muscular Dystrophies Muscular Dystrophy Musculoskeletal Diseases Myelitis Nervous System Diseases Neurodegenerative Diseases Neuroinflammatory Diseases Neuromuscular Diseases Picornaviridae Infections Poliomyelitis Post-Polio Syndrome Postpoliomyelitis Syndrome RNA Virus Infections Spinal Cord Diseases Spinal Cord Injuries Spinal Cord Injury Trauma, Nervous System Virus Diseases Wounds and Injuries

Age range

45 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Washington

Seattle, Washington, 98195, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Enhance Wellness

Behavioral

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

Primary outcomes

  1. Questionnaire: Level of reported self-efficacy as measured by the University of Washington Self-Efficacy Scale Questionnaire

    Time frame: 6-months

    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.

  2. Questionnaire: Patient Reported Outcome Measurement Information System (PROMIS) Pain Interference Short Form

    Time frame: 6-months

    Self-reported measure of pain interference. Greater score indicate greater pain interference.

  3. Questionnaire: Patient Reported Outcome Measurement Information System (PROMIS) Depression Short Form

    Time frame: 6-months

    Self-reported measure of depression. Greater scores indicated greater depressive symptoms.

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Registry information

Official study title

Project Enhance for Adults Aging With Long-Term Physical Disability

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
Jun 28, 2016
Registry last updated
Apr 3, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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