From identification of biopsychosocial risk factors to an increase in pain-related self-efficacy – the online-based conveyance of an explanatory model for persistent back pain

From identification of biopsychosocial risk factors to an increase in pain-related self-efficacy – the online-based conveyance of an explanatory model for persistent back pain - IDRIS

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

DRKS

Registry ID

DRKS00025445

Enrollment

564

Registered

2021-12-23

Start date

2022-11-30

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

F45.41 M54 F45.0 F45.8

Interventions

Group 1: Personalized psychoeducation regarding back pain Group 2: Treatment as usual (TAU)

Eligibility

Sex/Gender

All

Age

18 Years to 67 Years

Inclusion criteria

Inclusion criteria: Minimum burden of psychological distress due to symptoms operationalized as MCS-12 = 50; minimum burden symptom severity and symptom impairment (Numeric Rating Scale) = 5

Exclusion criteria

Exclusion criteria: Chronic back pain (>12 weeks of symptoms), substance use disorder, severe acute somatic back injury (herniated disc, surgical procedure, etc.), insufficient self-reported mental or physical health for study participation, lack of German language skills, current or previous inpatient psychosomatic hospital or rehabilitation treatment, current or previous outpatient psychotherapy due to back pain

Design outcomes

Primary

Measure	Time frame
Change in the patients' pain-specific self-efficacy after 1 month, determined via a questionnaire for the assessment of pain-specific self-efficacy (? FESS).	—

Secondary

Measure	Time frame
Change in intensity and impairment due to back pain after 1 and 3 months	—

Countries

Germany

Contacts

Public ContactPaul Hüsing

Klinik und Poliklinik für Psychosomatische MedizinUniversitätsklinikum Hamburg-Eppendorf

p.huesing@uke.de004940741053543

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 13, 2026