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Musculoskeletal Pain in Patients With Covid-19 Who Have Hospital Care

After the First and Second Wave in Italy: What Effects of Musculoskeletal Pain Did the Covid-19 in Patients Who Have Hospital Care?

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04632355
Acronym
Covid19-Pain
Enrollment
100
Registered
2020-11-17
Start date
2020-12-01
Completion date
2021-07-31
Last updated
2020-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19

Keywords

Covid19, Pain, musculoskeletal

Brief summary

Worldwide, the COVID-19 pandemic continues to grow. Although COVID-19 mainly affects the lungs and internal organs, musculoskeletal injury from this disease was reported with the presentation of marked elevation in creatine kinase and lactate dehydrogenase levels. Patients with post-acute COVID-19 are considered patients with a post-intensive syndrome (PICS) that results in loss of functional independence. In the physical and rehabilitation medical field, various modalities with therapeutic exercise can be used to manage pain by a physical therapist and psychiatrist. Pain management is particularly important during the COVID-19 pandemic because of the reduced accessibility to hospitals and medical resources.

Detailed description

The COVID-19 survivors with pain symptoms will participated. In this phase, a face-to-face interview will be conducted to collecting all outcomes about pain.

Interventions

OTHERInterview

This interview will be conducted to collecting all outcomes about musculoskeletal pain in COVID-19 survivors

Sponsors

Fondazione Don Carlo Gnocchi Onlus
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Recovered from COVID-19 infection. * COVID-19 survivors after hospitalization. * Musculoskeletal pain.

Exclusion criteria

* Participants will be excluded also if they score greater than 6 points on the Beck Depression Inventory (BDI) or more than 30 points in the State Trait Anxiety Inventory (STAI), dementia and not Italian speaking due to the high level of language skills required for questionnaires and quantitative sensory testing. * Psychiatric or neurological disorders

Design outcomes

Primary

MeasureTime frameDescription
Self-reported Version of the Leeds Assessment of Neuropathic Symptoms and SignsBaselinethe characterization of the pain. Total of 24. \> 11 neuropathic pain.
PainDETECBaselinethe characterization of the pain
EuroQol-5DBaselineTo measure quality of life, grade ranging from 0 (the worst possible health status) to 100 (the best possible health status)
The Hospital Anxiety and Depression ScaleBaselineTo measure psychological status. 0-7 = Normal; 8-10 = Borderline abnormal (borderline case), 11-21 = Abnormal (case)

Countries

Italy

Contacts

Primary ContactJorge H Villafañe, Ph.D
mail@villafane.it3395857563

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026