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Motor Control in Chronic Fatigue Syndrome and Fibromyalgia

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01686074
Recruitment Status : Completed
First Posted : September 17, 2012
Last Update Posted : September 20, 2017
Sponsor:
Collaborator:
St. Olavs Hospital
Information provided by (Responsible Party):
Norwegian University of Science and Technology

Tracking Information
First Submitted Date September 12, 2012
First Posted Date September 17, 2012
Last Update Posted Date September 20, 2017
Study Start Date September 2012
Actual Primary Completion Date December 2014   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: August 11, 2014)
motor control [ Time Frame: 1 day ]
Original Primary Outcome Measures Not Provided
Change History Complete list of historical versions of study NCT01686074 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Motor Control in Chronic Fatigue Syndrome and Fibromyalgia
Official Title Motor Control in Chronic Fatigue Syndrome and Fibromyalgia.
Brief Summary This project is a comprehensive study, with main focus on motor control, comparing patients with chronic fatigue syndrome / myalgic encephalopathy (CFS/ME) and/or fibromyalgia syndrome (FMS). Focus of the present project will be on detailed movement analysis in a movement laboratory and involve functional tasks such as walking and standing. Investigations will also comprise muscle activity, reaction time and fine motor control.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Case-Control
Time Perspective: Cross-Sectional
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Patients with chronic fatigue syndrome and fibromyalgia from primary care clinics.
Condition
  • Fibromyalgia
  • Chronic Fatigue Syndrome
Intervention Not Provided
Study Groups/Cohorts
  • Chronic fatigue syndrome
  • fibromyalgia
  • chronic fatigue syndrome + fibromyalgia
  • healthy sedentary control
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: March 10, 2015)
90
Original Estimated Enrollment
 (submitted: September 14, 2012)
120
Actual Study Completion Date December 2014
Actual Primary Completion Date December 2014   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Diagnosis of chronic fatigue syndrome or fibromyalgia

Exclusion Criteria:

  • patients who already had been treated.
Sex/Gender
Sexes Eligible for Study: All
Ages 19 Years to 49 Years   (Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Norway
Removed Location Countries  
 
Administrative Information
NCT Number NCT01686074
Other Study ID Numbers 2012/679
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Norwegian University of Science and Technology
Study Sponsor Norwegian University of Science and Technology
Collaborators St. Olavs Hospital
Investigators
Study Director: Egil A Fors, MD prof Norwegian University of Science and Technology
PRS Account Norwegian University of Science and Technology
Verification Date February 2017