2.1.7 Blinding

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A. Background & Definitions

Blinding refers to the masking of the treatment allocation for person(s) who perform the experiment, collect data and assess outcome. Blinding aims to make sure that someone has no knowledge about treatment allocation that may systematically influence his/her performance. The intended result is the equal treatment (as far as possible) of all experimental units (animals, subjects or samples) in the experiment.

In the discussion below, experimental groups refer to all groups involved in an experiment, for example: control, sham, treated with drug A, treated with drug B, etc.

Group allocation describes which experimental unit (animal, subject or sample) has been allocated to which experimental group.

The group allocation, actions and outcome assessments are ‘blinded’. People are ‘blind’ to particular information.

Blinding requires at least 2 people, one blinded person (unaware of experimental condition) and an unblinded person (knows the experimental condition and the blinding code). The unblinded person is the keeper of the blinding code which needs to be concealed until all processes under blinding are concluded.

The most effective blinding covers every step in an experiment - from allocation to treatment conditions, application of treatment to data collection and analysis - this is often referred to as full blinding.

Blinding should not be seen as "all or none". There are several situations when partial blinding may be applied (i.e. blinding of the most risk-prone step(s) in the experimental process). For example, partial blinding can be considered when:

• a research unit with no prior experience with blinding is introducing a blinding procedure and, for organizational or other reasons, follows a stepwise implementation
• a research unit has significantly constrained human resources and does not intend to conduct knowledge-claiming research

In any case, full and transparent reporting of how blinding was applied is expected.

​B. Guidance & Expectations

​​EQIPD expects that the method(s) to implement blinding are described with as much details as possible:

• either as a dedicated protocol (please see below for a template that may serve as an example on how to build such a protocol),
• or as a separate section of a study plan.

Dependent on the breadth of research methods in use, a given research unit may have one or more blinding protocols that can support blinding for specific types of experiments.

When preparing a blinding protocol, the main objective is to have a description that is understandable for the actual users - i.e. bench scientists (especially, those that are new to the unit). Therefore, it should be written in a simple language with as many examples (specific to the research) as appropriate.

A blinding protocol may describe the following:

• Training and competence
  • is there any training needed?
  • are there any additional supporting tools or materials available?

• Feasibility assessment (to avoid applying blinding when it makes no sense or would actually do harm)
  • how high is the risk of unintentional unblinding?
  • are the required resources available?
  • are emergency scenarios considered?

• "Who does what?"
  • for those involved in the experiment and the blinding procedure, are the roles clearly defined? (e.g. see section 4 in the blinding protocol template below);
  • from the blinding protocol, it should be clear who is aware of the group allocation at the different stages of the experiment (during the allocation, the conduct of the experiment, the outcome assessment, and the data analysis);
  • to effectively blind a study, create a sequence containing all experimental steps of the study and, for each step, indicate the name of each person involved in the conduct and analysis of the study. For each experimental step, document for each person whether they are blinded or not blinded to the condition or not involved at all. Such an overview systematically creates a transparent workflow of blinded and unblinded personnel and shows when unintended unblinding might occur. Such overview (e.g. as a table) can be made part of experimental documentation and reporting.
  • it is generally expected and strongly recommended that any process using humans as perceptors, raters or interpreters needs to be blinded until the decision-making is concluded.

• Blinding code
  • how is the blinding code developed and which specific steps are taken to practically apply it?
  • one simple blinding strategy is to assign each subject / sample a separate number of letter (or a combination thereof). This approach may create compliance issues in case of a large number of subjects / samples and the need to apply treatment repeatedly over extended periods of time.
  • another blinding strategy is to assign each when human processing and rating is involved in outcome assessment. The assessor may not know the condition behind the code but the knowledge of a group affiliation of a sample is a bias that can influence rating. This should be avoided.

If possible, check whether it is possible to use a blinding scheme without repeating codes. This is can be easily done with alphanumeric code consisting of 4 letter/number combinations, such as T7Z4. Such codes can be easily generated in Excel​

=CHAR(RANDBETWEEN(65;))&RANDBETWEEN(0;9)&CHAR(​RANDBETWEEN(65;))&RANDBETWEEN(0;9)​

Enter this formula in a row of cells for which you need coded samples. Copy the outcome to another worksheet with the command Past Special-->Paste Values.

Allocation concealment in animal experiments

The investigator shall not be aware and/or have the choice to which treatment group an animal is allocated to. This prevents selection bias. Therefore, the assignment to a specific group needs to be concealed and every animal should have the same chance to be assign to each of the groups. This can be achieved separating the assignment of animal_IDs to each animal (e.g. individual ear mark or subcutaneous chip) and randomization of treatments (see randomization) into two independent processes and then merge the two.

Effective blinding code

There are certain strategies to apply blinding.

RISK ASSESSMENT

• Under some circumstances, unintentional unblinding (e.g. due to a different appearance of a positive control in solution or suspension) may be a risk to be assessed and/or controlled
• Experimental treatments may produce adverse effects and attending veterinarians and animal care stuff may need to be informed in advance about the possibility of such adverse effects occurring and, if necessary, have emergency access to the blinding protocol.
• if a blinding code is added to another code such as animal_ID, measurement_ID or file name, watch out for hidden cues in such IDs, containing temporal or sequential information that could increase rater bias. Also metadata, such as creation date and time of a file containg measurements can give away experimental conditions.

PLEA​​SE DO NOT FORGET​

• Blinding is sometimes not possible especially when certain cues cannot be blinded, such as skin color of transgenic mice or color of a solution in a well. It is important to document this and to communicate in reports where blinding could or could not be achieved.
• ​Unblinding of the experimental conditions should be done when all blinded processes for the entire study are concluded. Early and partial unblinding for "checking" should be avoided and, if necessary, be part of the study protocol.
• Control group(s) (e.g., positive control group) should not be excluded from the blinding procedure.
• Provide training on how to apply the blinding procedure.

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C. Resources​

Guidelines on reporting of blinding (in vivo research):

• ARRIVE 2.0 ​​​

Template to develop a written description of the method used to implement blinding:

• [blinding protocol]

Reading material:

• Handbook of Experimental pharmacology chapter on randomization and blinding

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