Plaugher Gregory, Long Cynthia R, Alcantara Joel, Silveus Alyssa D, Wood Herbert, Lotun Kapildeo, Menke J Michael, Meeker William C, Rowe Stephen H
Director of Research, Life Chiropractic College West, 25001 Industrial Boulevard, Hayward, CA 94545, USA.
J Manipulative Physiol Ther. 2002 May;25(4):221-39. doi: 10.1067/mmt.2002.123171.
To determine the feasibility of conducting a randomized clinical trial in the private practice setting examining short- and long-term effects of chiropractic adjustments for subjects with essential hypertension compared with a brief soft tissue massage, as well as a nontreatment control group.
Randomized controlled-comparison trial with 3 parallel groups.
Private practice outpatient chiropractic clinic.
Twenty-three subjects, aged 24 to 50 years with systolic or diastolic essential hypertension.
Two months of full-spine chiropractic care (ie, Gonstead) consisting primarily of specific-contact, short-lever-arm adjustments delivered at motion segments exhibiting signs of subluxation. The massage group had a brief effleurage procedure delivered at localized regions of the spine believed to be exhibiting signs of subluxation. The nontreatment control group rested alone for a period of approximately 5 minutes in an adjustment room.
Cost per enrolled subject, as well as systolic and diastolic blood pressure (BP) measured with a random-0 sphygmomanometer and patient reported health status (SF-36). Pilot study outcome measures also included an assessment of cooperation of subjects to randomization procedures and drop-out rates, recruitment effectiveness, analysis of temporal stability of BPs at the beginning of care, and the effects of inclusion/exclusion criteria on the subject pool.
Thirty subjects enrolled, yielding a cost of $161 per enrolled subject. One subject was later determined to be ineligible, and 6 others dropped out. In both the chiropractic and massage therapy groups, all subjects were classified as either overweight or obese; in the control group there were only 2 classified as such. SF-36 profiles for the groups were similar to that of a normal population. The mean change in diastolic BP was -4 (95% confidence interval [CI]: -8.6, 0.5) in the chiropractic care group, 0.5 (95% CI: -3.5, 4.5) in the brief massage treatment group, and -4.9 (95% CI: -9.7, -0.1) in the no treatment control group. At the end of the study period, this change was -6.3 (95% CI: 13.1, 0.4), -1.0 (95% CI: -7.5, 15.6), -7.2 (95% CI: -13.3, -1.1) in the 3 study groups. The mean improvements in the chiropractic care and no treatment control groups remained consistent over the follow-up period.
This pilot study elucidated several procedural issues that should be addressed before undertaking a full-scale clinical trial on the effects of chiropractic adjustments in patients with essential hypertension. A multidisciplinary approach to recruitment may need to be used in any future efforts because of the limited subject pool of patients who have hypertensive disease but are not taking medications for its control. Measures need to be used to assure comparable groups regarding prognostic variables such as weight. Studies such as these demonstrate the feasibility of conducting a full-scale 3-group randomized clinical trial in the private practice setting.
确定在私人诊所环境中开展一项随机临床试验的可行性,该试验旨在研究脊椎按摩疗法对原发性高血压患者的短期和长期影响,并与简短的软组织按摩以及非治疗对照组进行比较。
具有3个平行组的随机对照比较试验。
私人诊所门诊脊椎按摩诊所。
23名年龄在24至50岁之间的收缩期或舒张期原发性高血压患者。
为期两个月的全脊柱脊椎按摩护理(即冈氏整脊法),主要包括在显示半脱位迹象的运动节段进行特定接触、短杠杆臂调整。按摩组在被认为显示半脱位迹象的脊柱局部区域进行简短的轻抚法操作。非治疗对照组在调整室单独休息约5分钟。
每个入组受试者的成本,以及使用随机零血压计测量的收缩压和舒张压(BP),以及患者报告的健康状况(SF-36)。初步研究的观察指标还包括对受试者参与随机化程序的合作情况和退出率的评估、招募效果、护理开始时血压的时间稳定性分析,以及纳入/排除标准对受试者群体的影响。
30名受试者入组,每个入组受试者的成本为161美元。后来确定1名受试者不符合条件,另外6名退出。在脊椎按摩疗法组和按摩治疗组中,所有受试者均被归类为超重或肥胖;对照组中只有2名被归类为此类。各小组的SF-36概况与正常人群相似。脊椎按摩护理组舒张压的平均变化为-4(95%置信区间[CI]:-8.6,0.5),简短按摩治疗组为0.5(95%CI:-3.5,4.5),非治疗对照组为-4.9(95%CI:-9.7,-0.1)。在研究期结束时,3个研究组的这一变化分别为-6.3(95%CI:13.1,0.4)、-1.0(95%CI:-7.5,15.6)、-7.2(95%CI:-13.3,-1.1)。脊椎按摩护理组和非治疗对照组的平均改善情况在随访期内保持一致。
这项初步研究阐明了在对原发性高血压患者进行脊椎按摩疗法效果的全面临床试验之前应解决的几个程序问题。由于患有高血压疾病但未服用控制药物的患者受试者群体有限,未来任何努力可能都需要采用多学科招募方法。需要采取措施确保各比较组在体重等预后变量方面具有可比性。此类研究证明了在私人诊所环境中开展全面的3组随机临床试验的可行性。