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NCT05894629

Effects of an Active Coping Program in Patients With Persistent Post-Covid Pain.

Completed NA Last updated 4 June 2025
What this trial tests

NA trial testing Pain Neuroscience Education (PNE)+ Therapeutic Exercise (TE) in Long COVID in 89 participants. Completed in 30 September 2023.

Timeline
20 February 2023
Primary endpoint
1 June 2023
30 September 2023

Quick facts

Lead sponsorUniversity of Valladolid
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment89
Start date20 February 2023
Primary completion1 June 2023
Estimated completion30 September 2023
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

University of Valladolid

Who can join

Adults 18 to 65, any sex, with Long COVID or Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Long COVID

Currently open trials in the same condition.

Other University of Valladolid trials

Trials by the same sponsor.

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Data sources for this page

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