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Mindfulness Meditation for Subjects With Severe Speech and Physical Impairments (MSPi)

Primary Purpose

Physical Impairments, Cerebral Palsy, Cerebral Ataxia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mindfulness Meditation Training
Audio Group
Sponsored by
Oregon Health and Science University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Physical Impairments focused on measuring Mindfulness, Meditation, acute lateral sclerosis, Cerebral Palsy, Cerebral Ataxia, Locked-in Syndrome

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Have a diagnosis by a neurologist of acquired neuromuscular or neurodevelopmental disorder
  • be capable of participating in 2-hour experimental interactions
  • Be literate in English
  • Be English speaking but not be able to communicate by voice or sign language
  • Have normal or corrected vision and hearing
  • Have speech that is understood less than 25% of the time
  • Have reduced hand function for writing and typing

Exclusion Criteria:

  • Have full ability to communicate verbally and with writing/typing

Sites / Locations

  • Participant Homes

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mindfulness meditation training

Audio Group

Arm Description

6-week, one-on-one, mindfulness meditation intervention based on Mindfulness-Based Cognitive Therapy program

6 weeks of listening to podcasts daily (same length as guided meditations), and discussing podcast content with research assistant during weekly study visits

Outcomes

Primary Outcome Measures

Change from Baseline in Working Memory at 8 weeks (post intervention)
Computer-based working memory task, classically titled "N-Back" task. Participants watch a series of letters presented on a screen, one after the other, and they are instructed to watch for letters being repeated 1 back (two in a row), 2 back (one letter in between repeat), etc (adjusted according to ability).

Secondary Outcome Measures

Change from Baseline in Perceived Stress Scale at 8 weeks (post intervention)
Change from Baseline in performance on BCI spelling task at 8 weeks (post intervention)
Participants use a brain-computer interface system (with EEG) designed for letter-detection

Full Information

First Posted
July 9, 2013
Last Updated
April 11, 2017
Sponsor
Oregon Health and Science University
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1. Study Identification

Unique Protocol Identification Number
NCT01964664
Brief Title
Mindfulness Meditation for Subjects With Severe Speech and Physical Impairments
Acronym
MSPi
Official Title
Mindfulness Meditation for Subjects With Severe Speech and Physical Impairments
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oregon Health and Science University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this protocol is to (1) Determine whether a one-on-one mindfulness meditation intervention or audio training improves performance on an adaptive communication system that utilizes brain-computer interface (BCI); and (2) Determine whether the intervention reduces stress in subjects with severe speech and physical impairments (SSPI). Hypothesis: The group of subjects randomized to the mindfulness meditation training will improve BCI performance and stress levels more than the audio control group.
Detailed Description
Members of the research team will visit subjects' homes for 9 visits that will each last no longer than 2 hours. During the consenting process, participants may opt out of photograph/video recordings of their visits, and they will also be able to choose whether or not they would like their data to be stored in a repository. At the Initial visit, one or more research assistants will visit participants' homes to go over the consent with them and answer any questions they may have. Participants will then complete a computer-based attention task. For this task, they will watch letters flash quickly on a screen, and then they will be asked a "yes/no" question about each series of letters. The computer task will take 20-60 minutes, and the entire visit will last no longer than 2 hours. Researchers will return to participants' homes within two weeks to complete a Baseline visit. At this time, the investigators will administer the same computer-based attention task. The investigators will also do an EEG recording during a BCI "mastery task," in which participants will try to spell words by looking at a series of letters presented on computer screen. During the "mastery task," the investigators will take a recording called an electroencephalogram (EEG). Participants will be fitted with a cap (much like a swimming cap) with electrodes (small metal sensors that measure electricity). The investigators will place a small amount of electrode gel on the scalp at each electrode site. The "mastery task" will take no longer than 60 minutes. After the visit, participants will then be emailed an internet-based survey that takes approximately one hour to complete. They will be asked questions about self-perceived stress, feelings and emotions, sleep, how well they think they can pay attention, and their opinions about meditation. This will take approximately 1 hour to complete. After completing the online surveys, participants will be randomized to receive either an audio or meditation training. The first training is approximately 2 hours long. If they have been randomly selected to receive the audio training, they will listen to and discuss podcasts with the instructor. If they have been randomly selected to receive the meditation training, they will learn about mindfulness, do an awareness exercise, listen to a guided meditation, and receive mindfulness handouts. They will be given an iPod Touch with either podcasts or guided meditations on it (depending on the group assignment) for the duration of the class, along with headphones and/or speakers. Participants will be asked to do approximately 30 minutes of practice each day, or as much as they are able. They will be asked to record how much they practice. Though this is optional, many people find it helpful to keep a log of their practice. For others, it may feel too burdensome or infeasible. Participants will be able to choose whether or not they want to keep a record of their practice. The iPod Touch will record when and for how long they listen. At the end of the class, they will be given a CD with all of the guided meditations on it. If participants receive meditation trainings, the instructor will give them some questions to think about before the next visit. They may contemplate and share about the questions via email to whatever extent they choose. The instructor will respond to their emails if they have any urgent needs and talk with participants about their responses at the audio/meditation training visits. Throughout the study, regardless of which group participants are in, they may choose to communicate however much they like-it could be very little, or they may wish to spend several hours a week emailing reflections, observations, and questions about their audio/meditation practice. This is entirely up to individual participants. The investigators will go to participants home for five more meditation training sessions. For the meditation group, participants will be asked to do a meditation right before the instructor arrives. Each training session is about 90 minutes long. After the meditation/audio training has been completed, the investigators will conduct the Endpoint visit, which is the same as the Baseline visit and takes approximately 2 hours. It includes the "mastery task" and the computer-based attention task. After the visit, participants will be emailed the same online questionnaire about stress, emotions, sleep, attention, and meditation. This will take approximately 1 hour to complete. Participants will also be emailed some questions to get their feedback about how the research study went for them. Offering thoughtful responses to the questions will likely take approximately 30 minutes. After the baseline and endpoint, an online questionnaire will be emailed to the participants. It is a series of several surveys: the Perceived Stress Scale (PSS) is a 10-question instrument that utilizes a likert scale and measures self-perceived stress during the past week. The Positive and Negative Affect Scale (PANAS) will also be administered. It is also 10 questions and uses a likert scale. It consists of words that describe feelings and emotions, and participants are to indicate the extent to which they generally feel that way. The APT-II Attention Questionnaire gathers information about participants' self-perceived ability to pay attention. The Pittsburgh Sleep Quality Index (PSQI) asks questions about sleep. And the Attitudes Toward Study solicits information about participants' thoughts and feelings on meditation (the wording of the Pre- and Post- tests vary only slightly).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Physical Impairments, Cerebral Palsy, Cerebral Ataxia, locked-in Syndrome
Keywords
Mindfulness, Meditation, acute lateral sclerosis, Cerebral Palsy, Cerebral Ataxia, Locked-in Syndrome

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mindfulness meditation training
Arm Type
Experimental
Arm Description
6-week, one-on-one, mindfulness meditation intervention based on Mindfulness-Based Cognitive Therapy program
Arm Title
Audio Group
Arm Type
Active Comparator
Arm Description
6 weeks of listening to podcasts daily (same length as guided meditations), and discussing podcast content with research assistant during weekly study visits
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness Meditation Training
Intervention Description
6-week, one-on-one meditation training. 90-minute home study visit once per week with research assistant. Learn Mindfulness-Based Cognitive Therapy curriculum and mindfulness techniques, and are asked to practice guided meditations 30-45 minutes each day.
Intervention Type
Behavioral
Intervention Name(s)
Audio Group
Intervention Description
Listen to 30-minute podcasts on a daily basis, and discuss podcasts with research assistant at 90-minute weekly home visits. 6 weeks total.
Primary Outcome Measure Information:
Title
Change from Baseline in Working Memory at 8 weeks (post intervention)
Description
Computer-based working memory task, classically titled "N-Back" task. Participants watch a series of letters presented on a screen, one after the other, and they are instructed to watch for letters being repeated 1 back (two in a row), 2 back (one letter in between repeat), etc (adjusted according to ability).
Time Frame
Baseline and Endpoint (within 1.5 weeks pre and post intervention)
Secondary Outcome Measure Information:
Title
Change from Baseline in Perceived Stress Scale at 8 weeks (post intervention)
Time Frame
Baseline and endpoint, within 1.5 weeks before and after intervention
Title
Change from Baseline in performance on BCI spelling task at 8 weeks (post intervention)
Description
Participants use a brain-computer interface system (with EEG) designed for letter-detection
Time Frame
Baseline and Endpoint, within 1.5 weeks of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Have a diagnosis by a neurologist of acquired neuromuscular or neurodevelopmental disorder be capable of participating in 2-hour experimental interactions Be literate in English Be English speaking but not be able to communicate by voice or sign language Have normal or corrected vision and hearing Have speech that is understood less than 25% of the time Have reduced hand function for writing and typing Exclusion Criteria: Have full ability to communicate verbally and with writing/typing
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barry Oken, MD
Organizational Affiliation
Oregon Health and Science University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Participant Homes
City
Portland Metropolitan Area
State/Province
Oregon
ZIP/Postal Code
97236
Country
United States

12. IPD Sharing Statement

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Mindfulness Meditation for Subjects With Severe Speech and Physical Impairments

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