Expose or protect? A randomized controlled trial of exposure in vivo vs pain-contingent treatment as usual in patients with complex regional pain syndrome type 1

被引:98
作者
den Hollander, Marlies [1 ,2 ,6 ]
Goossens, Marielle [1 ,3 ]
de Jong, Jeroen [1 ,3 ,6 ]
Ruijgrok, Joop [3 ]
Oosterhof, Jan [4 ]
Onghena, Patrick [5 ]
Smeets, Rob [2 ,3 ,8 ]
Vlaeyen, Johan W. S. [1 ,7 ]
机构
[1] Maastricht Univ, Dept Clin Psychol Sci, POB 616, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Med Ctr, Dept Rehabil, Maastricht, Netherlands
[3] Maastricht Univ, Dept Rehabil Med, CAPHRI Sch Publ Hlth & Primary Care, Maastricht, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Phys Therapy, Nijmegen, Netherlands
[5] KU Leuven Univ Leuven, Res Grp Methods Individual & Cultural Differences, Affect & Social Behav, Leuven, Belgium
[6] Adelante Ctr Expertise Rehabil, Hoensbroek, Netherlands
[7] KU Leuven Univ Leuven, Res Grp Hlth Psychol, Leuven, Belgium
[8] Libra Rehabil & Audiol, Eindhoven, Netherlands
关键词
Pain-related fear; Avoidance; CRPS-I; Exposure in vivo; Cognitive-behavioral treatment; LOW-BACK-PAIN; CHRONIC MUSCULOSKELETAL PAIN; ADJUVANT PHYSICAL-THERAPY; FEAR-AVOIDANCE MODEL; NEUROPATHIC PAIN; FUNCTIONAL LIMITATIONS; PERCEIVED HARMFULNESS; NECK PAIN; REDUCTION; SCALE;
D O I
10.1097/j.pain.0000000000000651
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Complex regional pain syndrome type I (CRPS-I) highly affects patients' ability to perform daily life activities. Pain-related fear might be a key target to reduce disability in chronic pain. Current treatments aiming at reducing pain show little improvements on pain and disability, whereas novel exposure-based treatments targeting pain-related fears have shown to be promising. We conducted a randomized controlled trial (N=46) comparing exposure in vivo (EXP) with pain-contingent treatment as usual (TAU), for CRPS-I patients with at least moderate levels of pain-related fear. Primary outcome is self-reported disability, for upper and lower extremity, respectively. Secondary outcomes are self-reported pain-intensity, pain-catastrophizing, perceived harmfulness of physical activity, and health-related quality of life. Pretreatment to posttreatment and pretreatment to 6-month follow-up change scores were tested using randomization-based inference. EXP was superior to TAU in reducing upper extremity disability from pretreatment to posttreatment (between-group difference, 1.082; 95% confidence interval [CI], 0.563-1.601; P<0.001) and from pretreatment to 6-month follow-up (1.303; 95% CI, 0.917-1.690; P,<0.001). EXP was superior in reducing lower extremity disability from pretreatment to 6-month follow-up (3.624; 95% CI, 0.467-6.781; P-0.02), but not from pretreatment to posttreatment (3.055; 95% CI, -0.018 to 6.128; P=0.054). All secondary outcomes significantly favored EXP pretreatment to posttreatment, as well as pretreatment to 6-month follow-up. Exposure to daily activities shows to be more effective than a protective pain-contingent TAU in reducing self-reported disability in daily life of CRPS-I patients with at least moderate levels of pain-related fear.
引用
收藏
页码:2318 / 2329
页数:12
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