Results 91 to 100 of about 114,155 (256)

Placebo Response is Driven by UCS Revaluation: Evidence, Neurophysiological Consequences and a Quantitative Model [PDF]

open access: yesarXiv, 2016
Despite growing scientific interest in the placebo effect and increasing understanding of neurobiological mechanisms, theoretical modeling of the placebo response remains poorly developed. The most extensively accepted theories are expectation and conditioning, involving both conscious and unconscious information processing.
arxiv  

Impure placebo as an unsound concept and other problems in the paper by Howick et al. : [Comment] [PDF]

open access: yes, 2013
Howick et al. have reported the findings of a survey that addressed the use of placebos among primary care practitioners in the United Kingdom. They adopted methodology similar to that used in previous studies performed in other countries; however, the ...
Hemilä, Harri   +2 more
core  

The effect of omega-3 and vitamin D co-supplementation on glycemic control and lipid profiles in reproductive-aged women with pre-diabetes and hypovitaminosis D: a randomized controlled trial

open access: yesDiabetology & Metabolic Syndrome, 2020
Background Prediabetes can predispose the individual to type 2 diabetes in the long-term. The present study was conducted to determine the effectiveness of vitamin D and omega-3 co-supplementation on glycemic control and serum lipid profiles in women of ...
Masoumeh Rajabi-Naeeni   +3 more
doaj   +1 more source

Using instrumental variables to disentangle treatment and placebo effects in blinded and unblinded randomized clinical trials influenced by unmeasured confounders [PDF]

open access: yesarXiv, 2016
Clinical trials traditionally employ blinding as a design mechanism to reduce the influence of placebo effects. In practice, however, it can be difficult or impossible to blind study participants and unblinded trials are common in medical research. Here we show how instrumental variables can be used to quantify and disentangle treatment and placebo ...
arxiv  

Placebo design in WHO-registered trials of Chinese herbal medicine need improvements

open access: yesBMC Complementary and Alternative Medicine, 2019
Background Physical identical and pharmacological inert are the basic requirements for placebo design, which are essential in clinical trials to evaluate the efficacy of an intervention.
Xuan Zhang   +5 more
doaj   +1 more source

Problematic placebos in physical therapy trials [PDF]

open access: yes, 2016
The placebo controlled, randomised controlled trial is widely recognised as the gold standard design for providing evidence in health care. Yet controversies surrounding placebos persist, which include issues regarding ethics, legality, mechanisms, and ...
Beecher   +28 more
core   +2 more sources

Analysis of the Choice of Control in Acupuncture Clinical Trials Involving Patients with Breast Cancer

open access: yesJournal of Acupuncture Research
Control group selection in clinical trials is challenging, especially in acupuncture studies. A PubMed literature review of control groups in breast cancer acupuncture studies was performed and identified 67 studies for analysis.
Molly Siegel   +5 more
doaj   +1 more source

Placebo: Feeling Better, Getting Better, and the Problems of Mind and Body [PDF]

open access: yes, 2008
Over its history, medicine has vacillated between acknowledging placebo effects as important and trying to overcome them. Placebos are controversial, in part, because they appear to challenge a biocentric view of the scientific basis of medical practice.
Kihlstrom, John F.
core   +1 more source

Relieving acute pain (RAP) study: a proof-of-concept protocol for a randomised, double-blind, placebo-controlled trial

open access: yesBMJ Open, 2019
Introduction Physicians and other prescribing clinicians use opioids as the primary method of pain management after traumatic injury, despite growing recognition of the major risks associated with usage for chronic pain.
Thomas Scalea   +13 more
doaj   +1 more source

Point and interval estimation of the target dose using weighted regression modelling [PDF]

open access: yesarXiv, 2020
In a Phase II dose-finding study with a placebo control, a new drug with several dose levels is compared with a placebo to test for the effectiveness of the new drug. The main focus of such studies often lies in the characterization of the dose-response relationship followed by the estimation of a target dose that leads to a clinically relevant effect ...
arxiv  

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