Physical Activity and Fatigue in Myasthenia Gravis

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Completed
CT.gov ID
NCT03905473
Collaborator
(none)
779
1
16.3
47.7

Study Details

Study Description

Brief Summary

Danish patients with myasthenia gravis are asked to answer a validated and international questionnaire about physical activity. Also background questions about their disease and comorbidity are asked. To validate the data about physical activity from the questionnaires 69 patients are asked to wear an accelerometer for 7 days to measure activity level.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Accelerometer measurements

Detailed Description

Secure digital mails are sent to around1500 patients qua their civil registration number (CPR number) (each resident of Denmark has a permanent unique civil registration number that is provided at birth or immigration to Denmark). The mail contains a link for the software REDCap (© 2018 Vanderbilt University), recommended by Rigshospitalet. REDcap is a secure web application for building and managing online surveys and databases. Patients are, in REDcap, informed about the project, and if interested, asked to sign the included informed content and answer six validated and translated questionnaires.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
779 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Habitual Physical Activity in Patients With Myasthenia Gravis Assessed by Accelerometry and Questionnaire
Actual Study Start Date :
Jun 1, 2019
Actual Primary Completion Date :
Apr 10, 2020
Actual Study Completion Date :
Oct 10, 2020

Outcome Measures

Primary Outcome Measures

  1. Multidimensional Fatigue Inventory (MFI-20) [5 minutes]

    MFI-20 is a self-reported questionnaire that measures fatigue severity. It contains 20 items and consists of five fatigue domains: mental fatigue, reduced motivation, reduced activity, physical fatigue and general fatigue. The response options consist of five check boxes ranging from "Yes, that is true" to "No, that is not true". The scores in each domain range from 4 to 20, with higher scores indicating higher levels of fatigue. A total fatigue score for all five domains is not used. MFI-20 has been used in several clinical and healthy populations.

Secondary Outcome Measures

  1. The short International Physical Activity Questionnaire (IPAQ) [3 minutes]

    IPAQ short form is used to measure self-reported time spent on physical activity and sedentary behavior. The questionnaire measures four intensity levels of physical activity from none (sedentary) to strenuous physical activity. Patients are asked to report number of hours and minutes per day on the different activity levels.

  2. Insomnia Severity Index (ISI) [3 minutes]

    ISI measures self-reported sleep quality and disturbances during the previous 2 weeks. The ISI comprises seven items assessing the perceived severity of difficulties initiating sleep, staying asleep, and early morning awakenings, satisfaction with current sleep pattern, interference with daily functioning, noticeability of impairment attributed to the sleep problem, and degree of distress or concern caused by the sleep problem. Each item is rated on a scale from 0 - 4 from less to more severe. The total score is the sum of each individual item and can range from 0 to 28 (28= most severe).

  3. Myasthenia gravis activity of daily living profile (MG-ADL) [10 minutes]

    Impact on daily living is assessed using the MG-ADL. An eight-question survey of symptoms severity, with each response graded from 0 (normal) to 3 (most severe). Questions include ocular, oropharyngeal, respiratory, and extremity functions. Total MG-ADL score ranges from 0 to 24. MG-ADL is also an indirect measurement of disease severity.

  4. Myasthenia gravis quality of life 15-item score (MG-QoL15) [3 minutes]

    MG -specific quality-of-life instrument is a 15-item questionnaire encompassing physical and psychological domains of MG to assess disease-specific Qol in MG patients. Rating consist of a 5-point scale ranging from 0 ("not at all") to 4 ("very much") as to the degree to which patients agree with the given statement summing up to a total score 0-60 points.

Other Outcome Measures

  1. Gender [5 seconds]

    Are you a woman or a man?

  2. Verification of the MG status. [5 seconds]

    Are you diagnosed with MG? (Yes/no/ maybe - still under examination)

  3. Age [5 seconds]

    How old are you? (unit: years)

  4. Job [5 seconds]

    How is your actually job status? (working fulltime/ working part time, student, retired, out of work, early retiree, sick leave).

  5. Smoking [5 seconds]

    Are you a smoker? (Never, ex-smoker, daily smoker, smoker but not every day, using e-cigarettes, using nicotine products)

  6. Comorbidity [5 seconds]

    Are you suffering from any of these conditions? (depression, any other psychiatric disorder, any auto-immune disease, chronic obstructive pulmonary disease, any cardiac diseases, chronic fatigue, sleep apnoea)

  7. How many years diagnosed with MG? [5 seconds]

    Number of years since diagnosis.

  8. Symptoms of MG? [5 seconds]

    The patient register symptoms according to the Myasthenia Gravis Foundation of American clinical classification.

  9. Treatment for MG? [5 seconds]

    The patient report their pharmacological treatment for MG.

  10. Are you receiving immunoglobulin treatment or plasmaphereses? [5 seconds]

    Answer yes/no.

  11. Have you had a thymectomy? [5 seconds]

    Answer yes/no.

  12. Are you having any of these treatments? [5 seconds]

    The patient answer yes or no to the following treatments: benzodiazepine, antidepressant drugs or betablockers.

  13. Are you reguarly seen by a neurologist? [5 seconds]

    Answer yes/no

  14. How tall are you? [2 seconds]

    Answer in centimeter

  15. How much do you weight? [2 seconds]

    Answer in kilograms

  16. Are you living alone? [2 seconds]

    Yes/no

  17. Do you live with children? How many? [2 seconds]

    Answer in number of children

  18. Was is your highest education level? [2 seconds]

    Short/middle/high education level

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Danish resident.

  • Alive.

  • Minimum age 18 years.

  • Registered in the Danish Patient Register with diagnosis code 70.0 (ICD-10) or 733.09 (ICD 8).

  • Subscribing E-boks (the Danish system for receiving secure digital emails).

Exclusion Criteria:
  • I fulfilling the inclusion criteria, then no exclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 Rigshospitalet Copenhagen Denmark 2100

Sponsors and Collaborators

  • Rigshospitalet, Denmark

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Linda Kahr Andersen, Research Physiotherapist, Phd student, Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT03905473
Other Study ID Numbers:
  • H-18031231 1
First Posted:
Apr 5, 2019
Last Update Posted:
Mar 10, 2021
Last Verified:
Mar 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Linda Kahr Andersen, Research Physiotherapist, Phd student, Rigshospitalet, Denmark
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 10, 2021