Nonsurgical Korean Integrative Treatments for Symptomatic Lumbar Spinal Stenosis: A Three-Armed Randomized Controlled Pilot Trial Protocol

被引:3
|
作者
Kim, Kiok [1 ]
Shin, Kyung-Min [2 ]
Lee, Jun-Hwan [2 ,3 ]
Seo, Bok-Nam [4 ]
Jung, So-Young [2 ]
Youn, Yousuk [1 ]
Lee, Sang Ho [1 ]
Kim, Jaehong [1 ]
Qu, Wenchun [5 ,6 ]
Kim, Tae-Hun [7 ]
机构
[1] Mokhuri Neck & Back Hosp, Dept Spine Ctr, Seoul 06272, South Korea
[2] Korea Inst Oriental Med, Clin Res Div, Daejeon 34054, South Korea
[3] Univ Sci & Technol, Korean Med Life Sci, Daejeon 34113, South Korea
[4] Korea Inst Oriental Med, Mibyeong Res Ctr, Daejeon 34054, South Korea
[5] Mayo Clin, Dept Phys Med & Rehabil, Rochester, MN 55905 USA
[6] Mayo Clin, Div Pain Med, Dept Anesthesiol, Rochester, MN 55905 USA
[7] Kyung Hee Univ, Korean Med Hosp, Korean Med Clin Trial Ctr, Seoul 02447, South Korea
关键词
PAIN; VALIDATION; MEDICINE; SURGERY; VERSION;
D O I
10.1155/2016/2913248
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
This is a study protocol for a pilot three-armed randomized controlled trial on nonsurgical integrative Korean medicinal treatment for symptomatic lumbar spinal stenosis (LSS). Thirty-six participants who have been diagnosed with (LSS) and recommended for spinal surgery by neurosurgeons or orthopedics and have had spinal symptoms such as severe low back pain and neurological claudication regardless of at least three months of conservative treatments will be recruited. Participants will be randomly assigned to be one of the three intervention groups, including the Mokhuri treatment program group 1 or 2 or usual care group. All treatments will be administered in inpatient units over a period of 4 weeks. The primary outcomes are 0 to 100 Visual Analogue Scales for low back pain and leg pain and the secondary outcomes are Oswestry Disability Index; EQ-5D; Roland-Morris Disability Questionnaire; Oxford Claudication Score; physical function test, including treadmill test, walking duration, and distance assessment for free leg pain; radiologic testing; and adverse events which will be assessed during the 4-week treatment period as well as after 3 and 6 months of follow-up. Then, we will assess the feasibility of the clinical trial design as well as a nonsurgical integrative treatment program. This trial is registered with CRIS registration number: KCT0001218.
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页数:7
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