TY - JOUR
T1 - Practice-based randomized controlled-comparison clinical trial of chiropractic adjustments and brief massage treatment at sites of subluxation in subjects with essential hypertension
T2 - Pilot study
AU - Plaugher, Gregory
AU - Long, Cynthia R.
AU - Alcantara, Joel
AU - Silveus, Alyssa D.
AU - Wood, Herbert
AU - Lotun, Kapildeo
AU - Menke, J. Michael
AU - Meeker, William C.
AU - Rowe, Stephen H.
N1 - Funding Information:
This pilot study was funded by grant no. 94-03-09 from the National Chiropractic Mutual Insurance Company and administered by the Foundation for Chiropractic Education and Research, Brookline, MA. Additional funding was provided by a grant from the Chiropractic Centennial Foundation, Davenport, Iowa, as well as professional support from the Palmer Center for Chiropractic Research, Davenport, Iowa, Life Chiropractic College West, Hayward, California, and the Gonstead Clinical Studies Society, Smyrna, Georgia. The data collected in this study occurred while the principal investigator (G.P.) was an assistant professor at Palmer College of Chiropractic West, San Jose, California, and a Visiting Research Fellow at the Palmer Institute for Graduate Studies and Research in Davenport, Iowa, during the years 1994 to 1995.
PY - 2002/5
Y1 - 2002/5
N2 - Objective: 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. Design: Randomized controlled-comparison trial with 3 parallel groups. Setting: Private practice outpatient chiropractic clinic. Patients: Twenty-three subjects, aged 24 to 50 years with systolic or diastolic essential hypertension. Interventions: 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. Main Outcome Measures: 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. Results: 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. Conclusions: 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.
AB - Objective: 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. Design: Randomized controlled-comparison trial with 3 parallel groups. Setting: Private practice outpatient chiropractic clinic. Patients: Twenty-three subjects, aged 24 to 50 years with systolic or diastolic essential hypertension. Interventions: 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. Main Outcome Measures: 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. Results: 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. Conclusions: 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.
KW - Cervical vertebrae
KW - Chiropractic
KW - Hypertension
KW - Lumbar vertebrae
KW - Pelvis
KW - Pilot study
KW - Randomized clinical trial
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U2 - 10.1067/mmt.2002.123171
DO - 10.1067/mmt.2002.123171
M3 - Article
C2 - 12021741
AN - SCOPUS:0036561073
SN - 0161-4754
VL - 25
SP - 221
EP - 239
JO - Journal of Manipulative and Physiological Therapeutics
JF - Journal of Manipulative and Physiological Therapeutics
IS - 4
ER -