Subjects
20 outpatients (women=15 men=5) with chronic low back pain (CLBP) were recruited by referrals from the hospital’s internal pain, orthopedic and neurological clinics, general practitioners and specialist doctors. The MBPT group was significantly younger (43 ±7.15 years) than the control group (54,5 ± 8.54 years, p<0,026 U-Test).
Intervention
Mindfulness-Based Pain Therapy (MBPT) is a program modeled by the first author after the curriculum developed by Kabat-Zinn et al. at the Stress Reduction Clinic of the University of Massachusetts Medical Center. As other mind-body approaches, MBPT focuses on increasing awareness and acceptance of present experience including physical distress and challenging thoughts and emotions.
Participants underwent individual intake interviews prior to admission in MBPT during which a short medical history was taken as well as informed consent procedures for participation in outcome research. Baseline measures were also obtained. Exclusion criteria included substance abuse, pregnancy, cognitive impairment, language barrier and severe mental disorders (such as psychotic symptoms). All participants were given usual medical care during the intervention.
Patients had no previous meditative experience. The intervention took place at the General Hospital of Klagenfurt am Wörthersee in Austria.
The study was approved by the medical ethics committee of the hospital of Klagenfurt am Wörthersee (Austria) (A12/19). All methods were performed in accordance with the relevant guidelines and regulations.
Frequency and Setting
MBPT-group was delivered by the first author, who is a MBSR trainer with extensive meditation teaching experience. An observing psychologist was also present at each session.
The control group was delivered by two licensed clinical psychologists of the general hospital of Klagenfurt with extensive experience in the multimodal pain therapy.
10 chronic pain patients (CLBP) were trained daily (2 h) in mindfulness meditation over a period of 4 weeks whilst the control group attended the standard multimodal pain management consisting of psychological group therapies, pain management and relaxation training, stress management training. Both groups received, from 8:00 a.m. to 12:00 a.m. medical therapies, coordination and endurance strength training as well as medical and psychological individual consultations.
Due to the relatively small number of participants available at a single time, it was not feasible to assign the participants randomly. For this reason, the allocation to treatment was based according to time of enrollment. The first 10 patients who enrolled were allocated to the control group, whereas the following 10 patients formed the MBPT-group.
Program techniques
The intervention was modeled closely by the first author after the MBSR program as taught at the University of Massachusetts Medical Center[i] and was delivered according to a manualized protocol. The MBPT program focuses specifically on chronic pain and involves a variety of mindfulness meditation techniques including: mindful breathing, body scan, mindful yoga, walking meditation, awareness of emotions and lovingkindness meditation (metta) practices as well as several techniques taken from cognitive therapy. Yoga was tailored to accommodate patients with chronic low back pain. MBPT differs from other mindfulness-based interventions (MBI) in that it entails more intensive daily meditative practice (at least 1 hour/day) 5 days per week. Moreover, participants were instructed to practice informal meditation, like being mindful in everyday activities (e.g. eating, walking, etc.). Daily class was divided between meditation practice, group discussions (in dyads or group). Written materials and recordings of guided meditations were provided, although participants were not explicitly instructed to practice at home. The didactic content included education about chronic pain, stress, sleep hygiene, functional and maladaptive pain-coping strategies, dysfunctional thoughts.
Adherence
One patient dropped out of the experimental group and one from the control group. Both dropped out due to unexpected family obligations. Program completion rate was very high (90%) a rate consistent with other studies.[ii] Compliance to MBPT class attendance was very high. Of a total of 19 classes only 3 patients missed one class.
1- and 3-month Follow-up
Of the 9 participants in the experimental group who completed the MBPT program 7 were available for 1-month and 3-month follow-up. In the control group 8 were available for 1-month follow-up and 7 for the 3-month follow up.
Data analysis
Descriptive statistics were used for the variables between MBPT group and control group. Appropriate parametric or non-parametric tests were done. Variables were compared by U-test (Wilcoxon rank-sum test) resp. 2-sample t test (Welch test) in case of normally distributed data. Normality was investigated by Kolmogoroff-Smirnov test.
The progression of the differences of the medians over the measurement time points was tested with the signed-rank test. Spearman rank correlation coefficient was calculated to examine association between scores.
Significance was defined as a p value less than 0.05. p values are reported to a maximum of three decimal places.
For all calculations the statistical package R version 4 resp. Hewlett-Packard RPL version 2.08 were used.
Measures
Numerical Pain Rating Scale
The Numerical Pain Rating Scale (NRS) is commonly used in clinical population in order to measure the intensity of pain. Patients choose before and after each session the number that best reflects the intensity of the pain, with 0 representing “no pain” and 10 indicating “worst pain imaginable”. Several studies provide evidence for its reliability and validity.[iii], [iv]
EuroQol 5-D
The EuroQol-5D (EQ-5D) questionnaire is an instrument which assesses health status. The EQ-5D comprises two components: Health state description and evaluation: The EQ-5D-description is a self-reported explanation of health problems according to a five-dimensional classification (mobility, self-care, usual activities, pain/discomfort and anxiety/depression).[v] In the EQ-5D-evaluation, the respondents report their health status using a visual analogue scale (VAS), comparable to a thermometer. Chronic pain is associated with overall decreased quality of life. The scale is graduated from 0 (the worst imaginable health state) to 100 (the best imaginable state). EQ-5D showed a good responsiveness to change after different interventions for CLBP patients.[vi]
Pain perception Scale PPS
The Pain Perception Scale (PPS)[vii] allows a differentiated assessment of perceived pain. It permits measurement of the emotional characterization and the sensory characterization of pain, uncoupling the physical sensation from the emotional and cognitive experience of pain.[viii] The questionnaire contains 24 items assigned in 5 subscales.
Pain disability index
The Pain disability index (PDI)[ix] is a self-report questionnaire which investigate how much pain interferes in different areas of patient’s life activity: such as family/home, recreation, social, occupation, sexual, self-care, life-support and average. The respondent uses a scale ranging from 0 (no disability) to 10 (maximum disability). The German PDI confirmed a good reliability and validity.[x]
Beck Depression Inventory II
Beck Depression Inventory II is a widely used 21-item self-report inventory for measuring the severity of depression.[xi] Numerous studies provide evidence for its reliability and validity.[xii] The German BDI-II shows good reliability and validity in clinical population.[xiii]
Pain Catastrophizing Scale
Pain Catastrophizing Scale PCS is a 13-item questionnaire that assesses catastrophizing, viewed as a multidimensional construct comprising rumination (“I can’t stop thinking about how much it hurts”), magnification (“I worry that something serious may happen”) and helplessness (“There is nothing I can do to reduce the intensity of the pain”).[xiv] The score ranges from 0 to 52. The German PCS represent a valuable tool in the assessment of German-speaking clinical population.[xv]