Ontology highlight
ABSTRACT: Objectives
In preclinical prognostic studies, the description of expected outcomes during an informed consent process indicates that the extent of pain and disability experienced and recovery time is unknown. In intervention studies, the consent process suggests that pain and disability will definitely occur and a treatment provided. Our objective was to determine whether study design (prognosis or intervention) was associated with the severity of pain intensity and disability reports from a preclinical model.Materials and methods
We pooled pain and disability outcomes from prognostic and intervention studies using an exercise-induced muscle injury model of pain. Pain intensity, disability, and fear of pain were collected by validated self-report measures. Pain and disabili
SUBMITTER: Bishop MD
PROVIDER: S-EPMC10243745 | biostudies-literature | 2023 Mar
REPOSITORIES: biostudies-literature