Ignite Creation Date:
2024-05-06 @ 7:06 PM
Last Modification Date:
2024-10-26 @ 3:00 PM
Study NCT ID:
NCT05894629
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2023-06-08
First Post:
2023-06-06
Brief Title:
Effects of an Active Coping Program in Patients With Persistent Post-Covid Pain
Sponsor:
University of Valladolid
Organization:
University of Valladolid
Study Overview
Official Title:
Effects of an Active Coping Program in Patients With Persistent Post-Covid Pain
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2023-06
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:
Justification among the sequelae of Covid-19 in clinical practice we frequently find persistent neuromusculoskeletal pain Previous studies carried out by this research group and in the scientific literature have shown that Pain Neuroscience Education PNE and Therapeutic Exercise TE constitute an effective care strategy in the treatment of persistent pain Therefore with this research we will try to respond with a treatment proposal from Primary Care PC
Objective to determine whether an PNE and TE program is effective in patients presenting Long Covid Pain LCP
Method Randomized clinical trial A sample of 80 subjects will be recruited The intervention group will receive a program of TE and PNE of 12 weeks duration 5 weeks of PNE of 1 weekly session of 90 minutes and 7 weeks of TE with a total of 19 sessions of 60 minutes duration The control group will receive the usual treatment An assessment will be made at the beginning and after the end of the intervention where the following variables will be measured quality of life intensity distribution and expansion of pain healthy physical condition and blood test values These will be evaluated by means of physical examination questionnaires and laboratory tests
Applicability of the expected results The proposed intervention is simple and reproducible It requires few resources and can produce changes in pain perception functionality and quality of life in patients with LCP
Objective to determine whether an PNE and TE program is effective in patients presenting Long Covid Pain LCP
Method Randomized clinical trial A sample of 80 subjects will be recruited The intervention group will receive a program of TE and PNE of 12 weeks duration 5 weeks of PNE of 1 weekly session of 90 minutes and 7 weeks of TE with a total of 19 sessions of 60 minutes duration The control group will receive the usual treatment An assessment will be made at the beginning and after the end of the intervention where the following variables will be measured quality of life intensity distribution and expansion of pain healthy physical condition and blood test values These will be evaluated by means of physical examination questionnaires and laboratory tests
Applicability of the expected results The proposed intervention is simple and reproducible It requires few resources and can produce changes in pain perception functionality and quality of life in patients with LCP
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