M54.5
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients (1.) who have reached the age of 18, (2.) have a registered diagnosis of low back pain M.54.5, (3.) have visited one of the practice locations because of their back pain during the study period. Additionally for the survey: who (4.) have consented to participate in the study, (5.) have the ability to answer the questionnaire independently, (6.) have the ability to understand the scope and significance of the study. Additionally for accelerometry: (7.) who are undergoing treatment in Bochum.
Exclusion criteria
Exclusion criteria: 1. non fulfillment of inclusion criteria will result in exclusion, 2. no understanding of the German language, 3. no comprehension/cognitive capacity to understand the study information letter and to give informed consent to study participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. secondary use of anonymous routine data of all patients diagnosed with M54.5 to describe the entire clientele and care practices: By using the statistics module of the practice management software MEDICAL OFFICE, different routine data can be extracted anonymously to describe the total sample and its care. Relevant data in the context of the present study are age and sex, insurance status, number and type of prescriptions/ remedies/ medications, and number and type of diagnostic procedures and surgeries. 2. online-based survey of patients with low back pain to collect further characteristics, needs and the further description of the care situation including their subjective evaluation: - Oswestry Disability Index -Numeric rating scale -Short Form Health Survey 12 -Tampa Scale for Kinesiophobia -Pain Catastrophizing Scale -Questionnaire on Physical Activity-Related Health Literacy -Neurophysiology of Pain Test -Client Satisfaction Questionnaire (CSQ-8)/ Zuf-8 -StarT Back -Patient Global Impression of change -German Pain Questionnaire (ausgewählte Items) -GEDA 2014/2015-EHIS (ausgewählte Items) 3. 7-day accelerometer measurement to evaluate physical activity in a randomly selcted subsample (in addition to survey): accelerometer measurement: amount of moderate to intense activity and energy expenditure over a 7-day period (ActiGraph GT3X+). The anticipated duration of the study is 3 months (equivalent to one quarter). | — |
Countries
Germany
Contacts
hsg Bochum - Hochschule für Gesundheit