Overlapping Pain Trajectory Study

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: Not specified

Inclusion Criteria

Inclusion Criteria: 1. General Criteria - Access to the internet either by laptop, tablet, or phone (for REDCap Surveys) - English-speaking - Parent or guardian willing to comply with protocol, complete study assessments, and provide written informed consent 2. Control Specific Criteria - No history/active chronic pain 3. Patient Specific Criteria - Patients will need a diagnosis of a chronic pain derived congruent with ICD-11 criteria related to headache (migraine, daily headache), abdominal (FAPD), localized MSK (single limb/joint, low back or chest pain), or diffuse MSK (widespread MSK pain) - If on medications, they need to be on stable doses of prescribed pain and/or psychiatric medications for 4 weeks before the baseline study visit. Exclusion Criteria: 1. General Criteria - Skin conditions (e.g., eczema) or past skin damage on the arms and legs in or near sites of sensory testing - Any comorbid rheumatic disease (e.g., arthritis, lupus), neurological (e.g., epilepsy, traumatic brain injury) or medical condition (e.g., cancer, diabetes) 2. Control Specific Criteria - Taking medications that can alter pain sensitivity (e.g., NSAIDs, opioids, stimulants, anticonvulsants; psychiatric) 3. Patient Specific Criteria - Present psychiatric disease as defined by DSM IV (e.g. psychosis, bipolar disorder, major depression, generalized anxiety disorder), alcohol or drug dependence, or documented developmental delays or impairments (e.g., autism, cerebral palsy, ADHD, or mental retardation) that, in the opinion of the investigator, would interfere with adherence to study requirements or safe participation in the study

Exclusion Criteria

Not provided

Study & Design

Study Type: Observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Conditioned Pain Modulation (CPM) Profile (Pressure);Conditioned Pain Modulation (CPM) Profile (Heat);Offset Analgesia (OA) Profile;Temporal Summation (TS) Profile;Spatial Summation (SS) Profile

Secondary Outcome Measures