Does group-based cognitive therapy improve functional ability, pain, catastrophic thoughts and quality of life in patients with persistent low back pain and psychological risk factors? A randomised controlled trial in a secondary care setting

被引:6
|
作者
Rolving, Nanna [1 ,2 ,3 ]
Agerbo, Karina [2 ]
Clausen, Stine Aalkjaer [2 ]
Denby, Kate Ane Rauff [2 ]
Jacobsen, Anna Puk [4 ,5 ]
Langagergaard, Vivian [2 ,5 ]
机构
[1] Cent Denmark Reg, Corp Qual, DEFACTUM, Aarhus, Denmark
[2] Silkeborg Reg Hosp, Spine Ctr, Diagnost Ctr, Silkeborg, Denmark
[3] Aarhus Univ, Dept Publ Hlth, Aarhus, Denmark
[4] Aarhus Municipal, Dept Social Affairs & Employment, Aarhus, Denmark
[5] Godstrup Hosp, Dept Clin Social Med & Rehabil, Aarhus, Denmark
关键词
Low back pain; rehabilitation interventions; randomized controlled trial; psychological factors; disability; FEAR-AVOIDANCE; BEHAVIORAL INTERVENTIONS; MUSCULOSKELETAL PAIN; CLINICAL-PRACTICE; DISABILITY; VALIDATION; GUIDELINES; EXERCISES; MODEL; SCALE;
D O I
10.1177/02692155211056202
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective To investigate the effects of a group-based cognitive behavioural intervention for patients with persistent low back pain (LBP) and psychological risk factors referred to secondary care. Design A randomised controlled trial. Setting Silkeborg Regional Hospital, Denmark. Subjects A total of 136 participants with chronic LBP and psychological risk factors. Interventions Participants were randomised to the standard care group, including examination by a rheumatologist and/or a physiotherapist, or the intervention group, including standard care plus a multidisciplinary group-based pain management programme. Main measures Patient-reported outcomes were collected at baseline and after 6 and 12 months. The primary outcome was disability (Roland Morris Disability Questionnaire). Secondary outcomes included low back pain intensity, pain catastrophising, health-related quality of life, and sick leave. Results Among 136 participants, 68 (mean age: 41.7 years (SD 11.8)) were randomised to standard care and 68 (mean age: 46.0 years (SD 10.8)) were randomised to the intervention group. Except for age, baseline characteristics were comparable between groups. 12-month follow-up was completed by 92.6% in the intervention group and 80.9% in the standard care group. Both groups achieved significant improvements on disability, with a reduction of -4.8 points (SD 6.1) in the intervention group compared to -3.7 points (SD 5.2), resulting in an insignificant difference between groups. No significant differences were found in the secondary outcomes. Conclusion A group-based pain management programme was no more effective than standard care for patients with persistent LBP and psychological risk factors.
引用
收藏
页码:317 / 330
页数:14
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