Objectives: To explore the theoretical justification for blinding in randomized trials and make recommendations concerning the implementation and interpretation of blinded randomized trials. Study: Design and Setting A theoretical analysis was conducted of the potential for bias in randomized trials with successful blinding (ie, trials in which beliefs about allocation to treatment or control groups are independent of actual allocation). The analysis identified conditions that must be satisfied to ensure that blinding eliminates the potential for bias associated with beliefs about allocation. Results: Even when beliefs about allocation are independent of actual allocation, they can still cause bias. The potential for bias is eliminated ...
Randomized clinical trials (RCTs) are widely used as the gold standard for comparative medical studi...
Objective Randomized controlled trials are the standard method for comparing treatments because they...
‘Blinding’ involves concealing knowledge of which trial participants received the interventions from...
Objectives To explore the theoretical justification for blinding in randomized trials and make recom...
Blinding is a methodologic safeguard of treatment evaluation, yet severely understudied empirically....
AbstractBlinding is a methodologic safeguard of treatment evaluation, yet severely understudied empi...
It is widely believed that baseline imbalances in randomized clinical trials must necessarily be ran...
Assessing allocation concealment and blinding in randomised controlled trials: why bother? The scien...
The search for new treatments and testing of new ideas begins in the laboratory and then established...
The rich history of blinding in clinical trials spans a couple of centuries.1 Most researchers world...
Randomized controlled trials (RCT) are known as the best method to prove causality in spite of vario...
Randomization and blinding are important tools in determining the effectiveness of a new interventio...
Abstract Background Selective allocation of patients into the compared groups of a randomised trial ...
Background: This paper addresses one threat to the internal validity of a randomized controlled ...
BACKGROUND: Evidence based medicine aims to integrate scientific evidence, clinical experience, and ...
Randomized clinical trials (RCTs) are widely used as the gold standard for comparative medical studi...
Objective Randomized controlled trials are the standard method for comparing treatments because they...
‘Blinding’ involves concealing knowledge of which trial participants received the interventions from...
Objectives To explore the theoretical justification for blinding in randomized trials and make recom...
Blinding is a methodologic safeguard of treatment evaluation, yet severely understudied empirically....
AbstractBlinding is a methodologic safeguard of treatment evaluation, yet severely understudied empi...
It is widely believed that baseline imbalances in randomized clinical trials must necessarily be ran...
Assessing allocation concealment and blinding in randomised controlled trials: why bother? The scien...
The search for new treatments and testing of new ideas begins in the laboratory and then established...
The rich history of blinding in clinical trials spans a couple of centuries.1 Most researchers world...
Randomized controlled trials (RCT) are known as the best method to prove causality in spite of vario...
Randomization and blinding are important tools in determining the effectiveness of a new interventio...
Abstract Background Selective allocation of patients into the compared groups of a randomised trial ...
Background: This paper addresses one threat to the internal validity of a randomized controlled ...
BACKGROUND: Evidence based medicine aims to integrate scientific evidence, clinical experience, and ...
Randomized clinical trials (RCTs) are widely used as the gold standard for comparative medical studi...
Objective Randomized controlled trials are the standard method for comparing treatments because they...
‘Blinding’ involves concealing knowledge of which trial participants received the interventions from...