Chronic Primary Pain

2

Review clinical trials related to Chronic Primary Pain. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Hyperthermia in Patients With Chronic Primary Pain - Effects on Thermoregulation, Somatosensory System and Movement Evoked Pain

This study, in a quasi-experimental matched two-group pre-post design, investigates the effect of serial water-filtered whole-body hyperthermia on circadian core body temperature, the somatosensory system (nociception) and the movement evoked pain in healthy and patients with chronic primary pain (e.g., fibromyalgia). The intervention lasts 3 weeks with two treatment sessions per week.

Participants needed: 60
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Bern University of Applied SciencesUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Confirmed diagnosis of widespread pain (ICD-11 MG30.01) [+9]

Participation in other clinical studies [+7]

Status: Recruiting

Network-Based vs. Standardized Cognitive Behavioral Therapy in Chronic Primary Pain

Cognitive-behavioral therapy (CBT) has been shown to be an effective treatment for chronic primary pain (CPP), but overall effect sizes are small to moderate. Process orientation, personalization, and data-driven clinical decision-making may be able to address the heterogeneity among people with CPP and are thus promising ways to increase the effectiveness of CBT for CPP. In a previous study, the feasibility of personalized CBT for CPP using network analysis was investigated. Based on this work, the present study aims to compare this personalized CBT with a standardized CBT as treatment-as-usual condition. In a balanced repeated measures design, a personalized CBT intervention is compared with a standardized CBT intervention. Participants are patients with CPP in German outpatient clinics. Primary and secondary outcome measures (disability, treatment expectations, pain intensity, working alliance, and side effects) will be collected after each study period. In addition, a SCED with randomized baselines will be embedded in the study, in which changes in processes relevant to chronic pain will be evaluated.

Participants needed: 75
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Prof. Dr. Julia GlombiewskiUpdated: May 1, 2025Locations: 1
Eligibility criteria

main diagnosis of chronic pain (i.e. pain persists for at least 6 months and is... [+2]

acute hazard due to suicidality, substance abuse, and/or psychosis [+6]