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Exposure-based Treatment for Avoidant Back Pain Patients

Not Applicable
Completed
Conditions
Low Back Pain
Registration Number
NCT01484418
Lead Sponsor
Philipps University Marburg Medical Center
Brief Summary

Chronic low back pain often results in psychosocial and physical disability. A subgroup of these patients shows fear of (re)injury and avoidance behaviour leading to higher disability. The purpose of this study is to determine whether exposure in vivo is more effective in the treatment of fear avoidant chronic back pain patients than psychological treatment as usual (cognitive behavioural psychotherapy).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
68
Inclusion Criteria
  • Having at least 3 months back pain
  • Sufficient level on fear avoidance scores (TSK, Phoda)
  • Being German-speaking
  • Agreeing to participate, verified by completion of informed consent
Exclusion Criteria
  • Red flags
  • Pregnancy
  • Illiteracy
  • Psychoses
  • Alcohol addiction
  • surgeries during the last 6 months or planed surgeries
  • Specific medical disorders or cardiovascular diseases preventing participation in physical exercise
  • Participating in another psychotherapy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change from baseline in pain severity at 3 and 6 months after admissionfrom Pretest (admission) to Posttest (an expected average of 3 months after admission) to Follow-up (an expected average of 6 months after admission)

Numeric Rating Scale (NRS)

Change from baseline in pain disability at 3 and 6 months after admissionfrom Pretest (admission) to Posttest (an expected average of 3 months after admission) to Follow-up (an expected average of 6 months after admission)

Pain Disability Index (PDI) Quebec Back Pain Disability Scale (QBPDS)

Secondary Outcome Measures
NameTimeMethod
Change in physical activity from Pretest to two in-between timepoints to Posttest to Follow-up Timefrom Pretest (admission) to one in-between timepoint (an expected 10 weeks after admission) to Posttest (an expected average of 3 months after admission) to Follow-up (an expected average of 6 months after admission)

International Physical Activity Questionnaire(IPAQ)

Change in pain catastrophizing from Pretest to two in-between timepoints to Posttest to Follow-upfrom Pretest (admission) to one in-between timepoint (an expected 10 weeks after admission) to Posttest (an expected average of 3 months after admission) to Follow-up (an expected average of 6 months after admission)

Pain Catastrophizing Scale (PCS)

Change in quality of life from Pretest to two in-between timepoints to Posttest to Follow-upfrom Pretest (admission) to one in-between timepoint (an expected 10 weeks after admission) to Posttest (an expected average of 3 months after admission) to Follow-up (an expected average of 6 months after admission)

EuroQol (EQ-5D)

Change in fear avoidance from Pretest to two in-between time points to Posttestfrom Pretest (admission) to one in-between timepoint (an expected 10 weeks after admission) to Posttest (an expected average of 3 months after admission) to Follow-up (an expected average of 6 months after admission)

Tampa Scale of Kinesiophobia (TSK) Pain Anxiety Symptom Scale (PASS)

Change in emotional distress from Pretest to two in-between timepoints to Posttest to Follow-upfrom Pretest (admission) to one in-between timepoint (an expected 10 weeks after admission) to Posttest (an expected average of 3 months after admission) to Follow-up (an expected average of 6 months after admission)

Hospital Anxiety and Depression Scale (HADS)

Trial Locations

Locations (1)

Philipps University Marburg, Department of Clinical Psychology and Psychotherapy

🇩🇪

Marburg, Germany

Philipps University Marburg, Department of Clinical Psychology and Psychotherapy
🇩🇪Marburg, Germany

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