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Pain-related learning and memory processes in chronic pain - the role of stress-related burden and traumatic life events

Pain-related learning and memory processes in chronic pain - the role of stress-related burden and traumatic life events - PAININSTRESS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00030834
Enrollment
100
Registered
2022-12-06
Start date
2022-12-15
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Chronic pain patients with different degrees of stress-related burden

Interventions

Group 1: Chronic pain patients: clinical interview to characterize stress-related burden and associated symptoms Pain threshold determination and repeated application of experimental somatic pain sti

Sponsors

Abteilung für Medizinische Psychologie und Medizinische Soziologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Fluent German; BMI 18-30 kg/m2 Patients with chronic pain: existing diagnosis of a chronic pain disorder with a focus on the musculoskeletal and/or visceral system (with pain > 12 weeks)

Exclusion criteria

Exclusion criteria: All participants: General MRI exclusion criteria (epilepsy, claustrophobia, ferromagnetic implants or prostheses, non-removable braces or piercings, pacemaker, tattoos on neck or neck area, etc.); pregnancy or lactation; skin disease on upper body/trunk area (due to possible interference with electrode and thermode placement). Chronic pain patients: Tumor-related pain, neuropathic pain, oral and facial pain, migraine; substance abuse; severe psychiatric illness, especially psychotic or manic symptoms, severe acute depressive episode; neurological, oncological diseases; diabetes mellitus; regular use of opioids, tricyclic antidepressants, antipsychotics Healthy control group: any mental or physical illness, especially acute or chronic pain; regular use of medication (except contraceptives)

Design outcomes

Primary

MeasureTime frame
Repeated assessment of valence and fear in response to predictive cues (CS) and CS-US contingencies using visual analog scales (VAS) across experimental phases on the study day; VAS assessments of US intensity and unpleasantness; electrodermal activity, pupillometry (psychophysiological correlates of conditioned responses of autonomic nervous system); state anxiety and stress-associated parameters (questionnaires)

Secondary

MeasureTime frame
Somatic pain thresholds;; Changes in electrogastrogram signal (EGG) and heart rate variability (HRV) during learning and extinction phases; Explicit and implicit emotional and sensory memory (questionnaires/assessments); Hair and salivary cortisol, alpha-amylase (measures of acute and chronic stress) MRI examination prior to experimental day to elicit brain structure, structural and functional connectivity (neurobiological predictors of pain-related learning)

Countries

Germany

Contacts

Public ContactDominic Pundt

Abteilung für Medizinische Psychologie und Medizinische Soziologie

dominic.pundt@rub.de+49 234 32 27318

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026