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Low back pain in German primary care - qualitative process evaluation of a feasibility study evaluating a practice nurse-led behavioural intervention

Practice-nurse-led behaviour-intervention for low back pain in German primary care – qualitative process evaluation of a feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN33541376
Enrollment
15
Registered
2024-02-19
Start date
2012-07-27
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Chronic back pain Musculoskeletal Diseases

Interventions

In collaboration with a psychologist, psychotherapist and general practitioner, a training concept for chronic pain management based on behavioural principles was developed. Practice nurses from one g

Sponsors

Universitätsmedizin Rostock
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Between 18 and 65 years old 2. Suffered from back pain for at least 6 months 3. Able to perform the training cognitively and physically

Exclusion criteria

Exclusion criteria: 1. Migraine headaches 2. Severe concomitant illnesses 3. Severe underlying mental illnesses 4. Patients taking opiates were only included after direct consultation and consideration with the study team

Design outcomes

Primary

MeasureTime frame
Implementability of a training program for patients, which included five sessions of 90 minutes each and focused in particular on the practice of progressive muscle relaxation according to Jacobson, assessed using a qualitative research method (a semi-structured interview with the practice nurses and patients) after completion of the training cycle

Secondary

MeasureTime frame
1. Pain intensity is measured with the Brief Pain Inventory (BPI) at Pre-intervention, before the 1st training session (T0), Post-intervention, after the last training session (T2) and as a follow-up, 3-6 months after the end of the training (T3) 2. Mental and physical state of health is measured using the Short Form Health Survey (SF-12) at Pre-intervention, before the 1st training session (T0), Post-intervention, after the last training session (T2) and as a follow-up, 3-6 months after the end of the training (T3) 3. Symptoms of depression and anxiety are measured using the Hospital Anxiety and Depression Scale (HADS) at Pre-intervention, before the 1st training session (T0), Post-intervention, after the last training session (T2) and as a follow-up, 3-6 months after the end of the training (T3) 4. Coping strategies and pain acceptance are measured by the Chronic Pain Acceptance Questionnaire (CPAQ) at Pre-intervention, before the 1st training session (T0) and Post-intervention, after the last training session (T2) 5. Pain-related disability in daily life is measured using the Roland and Morris Disability Questionnaire (RMDQ) at Pre-intervention, before the 1st training session (T0), Post-intervention, after the last training session (T2) and as a follow-up, 3-6 months after the end of the training (T3)

Countries

Germany

Contacts

Public ContactGregor Feldmeier
gregor.feldmeier@med.uni-rostock.de+49 (0)381 494 2481

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026