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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03067025
Other study ID # 1000055719
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 7, 2018
Est. completion date September 16, 2019

Study information

Verified date November 2019
Source The Hospital for Sick Children
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Most youth with MS experience symptoms such as depression and fatigue. In addition, cognitive issues, especially with attention and memory occur frequently. However, little is known about interventions that might work to improve these symptoms. In other work, the investigators have shown that higher levels of physical activity are associated with lower levels of depression and fatigue. Importantly, sleep problems are frequently encountered in youth with MS, and were seen in 60% of surveyed youth with MS in the investigators preliminary work. Modifiable lifestyle factors such as sleep and physical activity (PA) may play a key role in ameliorating common symptoms in pediatric MS. However, sleep has not been objectively described in pediatric MS, and the relationship between PA and sleep is poorly understood. This study aims to address these gaps.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 16, 2019
Est. primary completion date September 16, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 10 Years to 18 Years
Eligibility Inclusion Criteria:

1. Children ages 10 to 17 years, 11 months;

2. MS diagnosis following standard definitions (IPMSSG);

3. Healthy controls will include any child without a history of disease or disability

Exclusion Criteria:

1. Inability to communicate or understand English;

2. Those within 30 days of a relapse;

3. Children who exhibit severe respiratory problems at baseline (e.g. use of tracheotomy)

Study Design


Intervention

Device:
Actigraphy
Actiwatch Spectrum Plus will be worn on the non-dominant wrist 24 hours/day for seven days. Actigraphy is a valid and reliable objective measure of sleep patterns, including sleep quality, duration, and timing when compared to polysomnography (PSG).

Locations

Country Name City State
Canada Hospital for Sick Children Toronto Ontario

Sponsors (3)

Lead Sponsor Collaborator
The Hospital for Sick Children Queen's University, University of Alabama at Birmingham

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sleep quality, duration and timing This will be determined by actigraphy, using the ActiwatchSpectrum Plus, worn on the non-dominant wrist 24 hours/day for seven days. Participants will also complete a sleep diary, the Children's Behavior Check List Sleep Composite, Children's Sleep Habits Questionnaire (CSHQ) and the Pediatric Sleep Questionnaire to derive contextual information about sleep and to identify sleep problems. 7 days
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Recruiting NCT04782466 - ATOMIC (Active Teens Multiple Sclerosis) Physical Activity Research Program N/A