Cited by 1,196Pain Management and Placebo EffectGastrointestinal motility and disordersAcupuncture Treatment Research Studies

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Components of placebo effect: randomised controlled trial in patients with irritable bowel syndrome

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Kaptchuk, Ted J, Kelley, John M, Conboy, Lisa A, Davis, Roger B, Kerr, Catherine E, Jacobson, Eric E, Kirsch, Irving, Schyner, Rosa N, Nam, Bong Hyun, Nguyen, Long T, Park, Min, Rivers, Andrea L, McManus, Claire, Kokkotou, Efi, Drossman, Douglas A, Goldman, Peter, Lembo, Anthony J·2008·BMJ

DOI 10.1136/bmj.39524.439618.25PMC PMC2364862

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Abstract

OBJECTIVE: To investigate whether placebo effects can experimentally be separated into the response to three components-assessment and observation, a therapeutic ritual (placebo treatment), and a supportive patient-practitioner relationship-and then progressively combined to produce incremental clinical improvement in patients with irritable bowel syndrome. To assess the relative magnitude of these components. DESIGN: A six week single blind three arm randomised controlled trial. SETTING: Academic medical centre. PARTICIPANTS: 262 adults (76% women), mean (SD) age 39 (14), diagnosed by Rome II criteria for and with a score of > or =150 on the symptom severity scale. INTERVENTIONS: For three weeks either waiting list (observation), placebo acupuncture alone ("limited"), or placebo acupuncture with a patient-practitioner relationship augmented by warmth, attention, and confidence ("augmented"). At three weeks, half of the patients were randomly assigned to continue in their originally assigned group for an additional three weeks. MAIN OUTCOME MEASURES: Global improvement scale (range 1-7), adequate relief of symptoms, symptom severity score, and quality of life. RESULTS: At three weeks, scores on the global improvement scale were 3.8 (SD 1.0) v 4.3 (SD 1.4) v 5.0 (SD 1.3) for waiting list versus "limited" versus "augmented," respectively (P<0.001 for trend). The proportion of patients reporting adequate relief showed a similar pattern: 28% on waiting list, 44% in limited group, and 62% in augmented group (P<0.001 for trend). The same trend in response existed in symptom severity score (30 (63) v 42 (67) v 82 (89), P<0.001) and quality of life (3.6 (8.1) v 4.1 (9.4) v 9.3 (14.0), P<0.001). All pairwise comparisons between augmented and limited patient-practitioner relationship were significant: global improvement scale (P<0.001), adequate relief of symptoms (P<0.001), symptom severity score (P=0.007), quality of life (P=0.01). Results were similar at six week follow-up. CONCLUSION: Factors contributing to the placebo effect can be progressively combined in a manner resembling a graded dose escalation of component parts. Non-specific effects can produce statistically and clinically significant outcomes and the patient-practitioner relationship is the most robust component. TRIAL REGISTRATION: Clinical Trials NCT00065403.

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Authors: Kaptchuk, T. J., Kelley, J. M., Conboy, L. A., Davis, R. B., Kerr, C. E., Jacobson, E. E., Kirsch, I., Schyner, R. N., Nam, B. H., Nguyen, L. T., Park, M., Rivers, A. L., McManus, C., Kokkotou, E., Drossman, D. A., Goldman, P., & Lembo, A. J.
Affiliations: Harvard University (US)
Endicott College (US)
Beth Israel Deaconess Medical Center (US)
University of Hull (GB)
University of North Carolina at Chapel Hill (US)
Corresponding author: Kaptchuk, Ted J
ORCID: Kaptchuk, Ted J
Kelley, John M
Conboy, Lisa A
Davis, Roger B
Kerr, Catherine E
Kirsch, Irving
Park, Min
Drossman, Douglas A
Lembo, Anthony J
Venue: BMJ
Publisher: BMJ
Published: 2008-04-03
Volume: 336
Issue: 7651
Pages: 999-1003
ISSN: 1756-1833 (ISSN-L)
0959-8138
DOI: 10.1136/bmj.39524.439618.25
PMC: PMC2364862
OpenAlex: W2038810061
Cited by: 1,196
References: 35
Citations by year: 2026: 32 · 2025: 48 · 2024: 49 · 2023: 53 · 2022: 56 · 2021: 78 · 2020: 70 · 2019: 78 · 2018: 75 · 2017: 80 · 2016: 72 · 2015: 66 · 2014: 77 · 2013: 76 · 2012: 60
FWCI: 38.88
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.bmj.org/licenses/tdm/1.0/terms-and-conditions.html (tdm)
Locations: BMJ (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion)
HighWire Press Open Archive (submittedVersion)
Funders: Beth Israel Deaconess Medical Center
Harvard University
National Institutes of Health (5r21at002564-02)
National Institute of Diabetes and Digestive and Kidney Diseases
National Center for Complementary and Alternative Medicine
National Center for Research Resources (RR 01032, M01RR001032)
Office of Behavioral and Social Sciences Research
National Center for Complementary and Integrative Health (R01AT004662, R21AT002860, 1R21 AT002564, K24AT004095, R01AT001414)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Pain Management and Placebo Effect
Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
Health Sciences › Medicine › Complementary and alternative medicine › Acupuncture Treatment Research Studies
Keywords: placebo effect, irritable bowel syndrome, sham acupuncture, patient-practitioner relationship, healing rituals, non-specific effects, symptom severity, quality of life, symptom relief, placebo-controlled trial design
MeSH terms: Adult, Female, Humans, Male, Waiting Lists, Acupuncture Therapy, Placebo Effect, Single-Blind Method, Treatment Outcome, Irritable Bowel Syndrome

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