Ignite Creation Date:
2024-05-06 @ 11:16 AM
Last Modification Date:
2024-10-26 @ 12:42 PM
Study NCT ID:
NCT03474705
Status:
COMPLETED
Last Update Posted:
2018-12-27
First Post:
2018-03-05
Brief Title:
Clinical Outcomes Viscoelastic Properties and Central Pain Mechanisms After Eccentric Training in NeckShoulder Pain
Sponsor:
University of Seville
Organization:
University of Seville
Study Overview
Official Title:
Clinical Outcomes Muscle Stiffness and Creep and Central Pain Mechanisms Are Improved After Eccentric Training in Female Computer Users With Chronic NeckShoulder Pain
Status:
COMPLETED
Status Verified Date:
2018-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Objectives The aims are to 1 evaluate the clinical impact of eccentric training in female computer users with chronic NSP 2 compare pressure hyperalgesia temporal summation of pain TSP and conditioned pain modulation CPM in female office workers with and without NSP and 3 assess changes in central pain responses after training
Methods In part A twenty office workers with NSP will be compared with 20 healthy controls In part B the NSP group will undergo a 5-week eccentric training program Participants will report their pain intensity and complete the Neck Disability Index and the Disabilities of the Arm Shoulder and Hand questionnaire Pressure pain thresholds PPTs will be assessed over the neck and forearm Cuff algometry will identify pain detection PDT and tolerance thresholds PTT TSP will be evaluated by visual analogue scale pain scores during 10 repetitive cuff stimulations CPM will be calculated as the difference in PDT with and without a conditioning painful stimulus Outcomes will be measured at baseline and post-intervention
Methods In part A twenty office workers with NSP will be compared with 20 healthy controls In part B the NSP group will undergo a 5-week eccentric training program Participants will report their pain intensity and complete the Neck Disability Index and the Disabilities of the Arm Shoulder and Hand questionnaire Pressure pain thresholds PPTs will be assessed over the neck and forearm Cuff algometry will identify pain detection PDT and tolerance thresholds PTT TSP will be evaluated by visual analogue scale pain scores during 10 repetitive cuff stimulations CPM will be calculated as the difference in PDT with and without a conditioning painful stimulus Outcomes will be measured at baseline and post-intervention
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None