Impact of a Structured Wellness Behavioral Intervention on Quality of Life in NMOSD

Description

This project aims to study whether a structured wellness program intervention can improve quality of life among people living with Neuromyelitis Optica Spectrum Disorder (NMOSD). This pilot will test a multi-modal wellness program tailored to NMOSD patients that includes services from physical therapists, dietitians, social workers, nurse practitioners and cognitive therapists. The trial will be designed as a randomized controlled trial, randomizing patients to immediately starting the program as well as a 6 month delayed start. The intervention would leverage an existing clinical comprehensive MS wellness program at the Corinne Dickinson for Multiple Sclerosis (MS) at Mount Sinai Medical Center. The primary endpoint of this study would be evaluating quality of life, as assessed by MS-Quality of Life -54.

Conditions

Neuromyelitis Optica Spectrum Disorder (NMOSD)

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Study Overview

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Study Details

Study overview

This project aims to study whether a structured wellness program intervention can improve quality of life among people living with Neuromyelitis Optica Spectrum Disorder (NMOSD). This pilot will test a multi-modal wellness program tailored to NMOSD patients that includes services from physical therapists, dietitians, social workers, nurse practitioners and cognitive therapists. The trial will be designed as a randomized controlled trial, randomizing patients to immediately starting the program as well as a 6 month delayed start. The intervention would leverage an existing clinical comprehensive MS wellness program at the Corinne Dickinson for Multiple Sclerosis (MS) at Mount Sinai Medical Center. The primary endpoint of this study would be evaluating quality of life, as assessed by MS-Quality of Life -54.

Impact of a Structured Wellness Behavioral Intervention on Quality of Life in NMOSD

Impact of a Structured Wellness Behavioral Intervention on Quality of Life in NMOSD

Condition
Neuromyelitis Optica Spectrum Disorder (NMOSD)
Intervention / Treatment

-

Contacts and Locations

New York

Corinne Goldsmith Dickinson Center for MS at Mount Sinai, New York, New York, United States, 10029

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Adults (age ≥18) with NMOSD diagnosed with 2015 NMOSD clinical criteria.
  • * All EDSS scores will be considered in order to make the intervention accessible to all patients regardless of disability.
  • * All patients regardless of treatment type will be considered.
  • * Age\<18
  • * Inability to voluntarily provide consent for study participation
  • * Inability to participate in study evaluation and/or endpoint measures, or participation in another concurrent randomized controlled trial or wellness based intervention.
  • * Any patients with a relapse within 30 days of randomization or any patients with medical restrictions on physical activity will be excluded.
  • * Any patients who begin stimulants and/or dalfampridine between enrollment and randomization will be excluded.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Icahn School of Medicine at Mount Sinai,

Sammita Satyanarayan, MD, PRINCIPAL_INVESTIGATOR, Icahn School of Medicine at Mount Sinai

Study Record Dates

2028-01