- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05048576
The Effect of Auditory Cues on Mood and Gait
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ali Boolani, PhD
- Phone Number: 5043195828
- Email: aboolani@clarkson.edu
Study Locations
-
-
New York
-
Potsdam, New York, United States, 13699
- Recruiting
- Clarkson University
-
Contact:
- Ali Boolani, PhD
- Email: aboolani@clarkson.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria:
Able to stand without an assistive device
- This study requires subjects to stand and to walk with the Delsys monitors, thus we are unable to use subjects who cannot stand without assistive devices.
- Delsys monitors are a wearable device that allows for comprehensive analysis of gait and balance. The sensors will be attached to the subject and they will be instructed to perform the gait test by walking for 5 minute intervals over the duration of 63 minutes. The Delsys will generate a report automatically that will then be analyzed.
Able to walk in 5-minute intervals over the duration of 63 minutes without assistive devices.
The objective of this study is to measure gait. Assistive devices change gait and limit our ability to measure gait.
• Subjects must be within the age of 18-45
Exclusion criteria:
- Impairment or inability to perform physical activity (e.g. walking) independently.
- Inability to walk for 2 minutes without pain or discomfort.
Neurological conditions (i.e. stroke or Parkinson's disease)
○ Many neurological conditions can potentially alter gait. Therefore, we are eliminating individuals in this group.
Recent (within 6 months) orthopedic surgery that impacts walking ability and balance, e.g. total joint replacement
○ The objective of this study is to measure gait and people with lower extremity injuries may have excessive variation in gait. Hence we will be eliminating them from this study.
Wound or absent sensation on plantar surface (bottom) of the subject's feet.
○ Subjects with this issue will have alterations and variations in gait due to sensory deficits and/or pain. They will not eligible for this study.
- Visual Impairment ○ Subjects must be able to read and visually recognize words. Therefore, subjects must have 20/40 (corrected) vision. Subjects who are blind cannot participate.
Day of testing eligibility
- Subjects must not have consumed caffeine within the last 12 hours
- Subjects must have slept >2 hours of their normal reported sleep time .
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Positive auditory cues
Participants will listen to the following auditory cues ~30 seconds apart Good job, you're doing awesome!
Keep up the good work!
You've got this!
You're almost done, just a few more minutes!
That's a great pace!
You're going strong!
Keep it up!
Nice work.
Great job!
Good stuff.
Keep it up.
You're doing an amazing job.
|
Terms to be used in positive reinforcement: Good job, you're doing awesome! Keep up the good work! You've got this! You're almost done, just a few more minutes! That's a great pace! You're going strong! Keep it up! Nice work. Great job! Good stuff. Keep it up. You're doing an amazing job. |
|
EXPERIMENTAL: Negative auditory cues
Participants will listen to the following auditory cues ~30 seconds apart You've got to walk faster than that.
You're so slow!
Why do you walk like that?
Did you learn how to walk yesterday?
You're doing terrible.
Who walks like that?
You have potential but you don't use it.
You'll never amount to anything.
You're not putting very much effort into this.
This is the worst pace you've had yet.
|
Terms to be used in negative reinforcement: You've got to walk faster than that. You're so slow! Why do you walk like that? Did you learn how to walk yesterday? You're doing terrible. Who walks like that? You have potential but you don't use it. You'll never amount to anything. You're not putting very much effort into this. This is the worst pace you've had yet. |
|
EXPERIMENTAL: Music
Participants will be allowed to select a streaming music station of their choice.
|
Participant's can choose their own music to play during this condition.
|
|
ACTIVE_COMPARATOR: Silence
Participants will walk in silence while wearing noise cancelling headphones.
|
No recordings will be played during this condition.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Profile of Moods Survey (POMS) Fatigue
Time Frame: change in fatigue from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0-20 scale with higher scores being worse outcome
|
change in fatigue from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Profile of Moods Survey (POMS) Vigor
Time Frame: change in vigor from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0-20 scale with higher scores being better outcome
|
change in vigor from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Profile of Moods Survey (POMS) Tension
Time Frame: change in tension from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0 to 20 scale with higher scores being worse outcome
|
change in tension from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Profile of Moods Survey (POMS) Depression
Time Frame: change in depression from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0 to 20 scale with higher scores being worse outcome
|
change in depression from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Profile of Moods Survey (POMS) Anger
Time Frame: change in anger from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0 to 20 scale with higher scores being worse outcome
|
change in anger from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Profile of Moods Survey (POMS) Confusion
Time Frame: change in confusion from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
-4 to 16 scale with higher scores being worse outcome
|
change in confusion from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Profile of Moods Survey (POMS) Total Mood Disturbance
Time Frame: change in total mood disturbance from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
-24 to 96 with higher scores being worse outcomes
|
change in total mood disturbance from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
State Mental Energy
Time Frame: change in state mental energy from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0 to 300 with higher scores being better outcomes
|
change in state mental energy from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
State Physical Energy
Time Frame: change in state physical energy from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0 to 300 with higher scores being better outcomes
|
change in state physical energy from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
State Mental Fatigue
Time Frame: change in state mental fatigue from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0 to 300 with higher scores being worse outcomes
|
change in state mental fatigue from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
State Physical Fatigue
Time Frame: change in state physical fatigue from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
0 to 300 with higher scores being worse outcomes
|
change in state physical fatigue from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Gait speed
Time Frame: change in gait speed from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
gait speed in meters/second
|
change in gait speed from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
|
Gait variability
Time Frame: change in variability from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
Variability in gait speed (reported as percent)
|
change in variability from baseline to 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes during walking
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ali Boolani, PhD, Clarkson University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 20-20.2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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