20 differences between Randomized Controlled Trial (RCT) and Quasi-experimental study design

There are multiple similarities and differences between Randomized Controlled Trial and Quasi Experimental Studies.

Similarities between RCT and quasi-experiments are:

  • These are both experimental study designs
  • Study participants in both studies are subjected to some type of treatment/intervention and control group
  • Some outcome of interest is measured
  • The researchers test whether differences in this outcome are related to the treatment/intervention or not.

However, there are some major differences between these two studies.

20 major differences between RCT and quasi-experimental studies are:

S.N.

   Randomized Controlled Trial (RCT)

   Quasi-experimental Studies

1. RCT is an experimental study design where the subjects in a population are randomly allocated to different groups Quasi Experimental is an experimental study design where the subjects in a population are non-randomly allocated to different groups
2. Also known as randomized study Also known as non-randomized study
3. Study populations are selected randomly Study populations are chosen
4. Randomization is the main ingredient of RCT Randomization is not the main ingredient of Quasi-experimental
5. RCTs are always prospective These studies are generally prospective in nature
6. It uses truly random method of allocating participants to different groups It uses quasi-random method of allocating participants to different intervention groups i.e. the method of allocating is not truly random
7. Have high scientific validity It has moderate scientific validity
8. It provides the best scientific evidence to any study Evidences generated from this design are relatively of low significance while compared to RCT
9. It is considered as a ‘Gold Standard’ against which other research designs should be judged. It is not considered as a ‘Gold Standard’
10. It is considered as an ideal design for evaluating both the effectiveness and side effects of interventions It is not considered as an ideal design for evaluating both the effectiveness and side effects of interventions
11. The major strength of this study design is that it avoids any possibility of selection bias in the trial The major strength of this study design is that it is practicable in all context and can ensure ethical considerations at all times
12. RCT can be used up to a point unless there is any real-world constraint for random assignment Quasi-experimental design is used when real-world constraints like ethical, political or logistical constraints do not allow for randomization
13. It can be used to assess and strongly claim the causal effect of any programs, policies or interventions It cannot be used to assess and strongly claim the causal effect of any programs, policies or interventions
14. RCT, also known as true experiment has probability samples Quasi-experiment has non-probability samples
15. RCTs cannot be conducted and are not realistic at all times due to some practical or ethical reasons E.g.: while conducting studies related to exposure of harmful chemicals, we cannot randomize people to receive the harmful chemicals. It can be conducted without violating ethical considerations
16. These are generally quite expensive These are generally less expensive
17. Random assignment in RCT neutralizes factors other than the independent and dependent variables, which makes it possible to directly infer cause and effect

 

We can claim causality in quasi-experimental studies. However, we can never be certain that we have controlled for all confounding sources
18. RCT increases the likelihood that the groups will be comparable in terms of variables that we recognize and measure along with in terms of variables that we cannot recognize and may not be able to measure In quasi-experiment we can increase the likelihood that the groups will be comparable in terms of variables that we recognize and measure but not in terms of variables that we cannot recognize and may not be able to measure
19. RCT provide chances to control for unobserved biases, with an assumption that randomization was free from bias Quasi-experiment provides less chances to control for unobserved biases
20. It has less potential for bias, or confounding, and study validity is not compromised It has relatively increased potential for bias, or confounding, and study validity is compromised

References and for More Information:

https://www.nber.org/reporter/summer03/angrist.html

https://www.sri.com/research-development/randomized-controlled-trials-quasi-experimental-designs

https://www.researchgate.net/post/What_is_the_difference_between_experimental_and_quasi-experimental_research

https://medium.com/netflix-techblog/quasi-experimentation-at-netflix-566b57d2e362

https://www.researchconnections.org/childcare/datamethods/experimentsquasi.jsp

https://www.quora.com/What-are-the-differences-between-an-experimental-and-a-quasi-experimental-design

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2446460/

http://www.3ieimpact.org/media/filer_public/2012/05/14/mgaarderexperimentalquasiexperimentaldesignsjan2010.pdf

https://www.airmedicaljournal.com/article/S1067-991X(06)00286-0/pdf

http://samples.jbpub.com/9780763789961/89961_CH03_Macha.pdf

https://www.annualreviews.org/doi/pdf/10.1146/annurev-publhealth-040617-014128

http://www.understandingresearch.com/glossary/study-design-terms

https://www.med.uottawa.ca/sim/data/Study_Designs_e.htm

https://www.unicef-irc.org/KM/IE/img/downloads/Quasi-Experimental_Design_and_Methods_ENG.pdf

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669452/

http://www.scielo.sa.cr/scielo.php?script=sci_arttext&pid=S2215-35352015000200020

https://qualitysafety.bmj.com/content/qhc/12/1/47.full.pdf

http://www.bandolier.org.uk/booth/glossary/RCT.html

 

About Kusum Wagle 214 Articles
Hello and greetings everyone! I am Kusum Wagle, MPH, WHO-TDR Scholar, BRAC James P. Grant School of Public Health, Bangladesh. I have gained profound experiences in public health sector under different thematic areas of health, nutrition, sexual and reproductive health, maternal and newborn health, research etc., targeting diverse audience of different age groups. I have performed diverse roles ranging from lecturer in the public health department of colleges, nutrition coordinator, research coordinator and consultant, in different programs, projects and academic institutions of Nepal. I also hold immense experience in working closely and persistently with government organizations, non-government organizations, UN agencies, CSOs and other stakeholders at the national and sub-national level. I have successfully led and coordinated different projects involving multi-sector participation and engagement. Moreover, I am also regularly involved in the development of different national health related programs and its guidelines.