Treatment FAQ

what does it mean when both control and treatment groups have the same slop?

by Giovani Thompson Published 2 years ago Updated 2 years ago

What is the control group in a research study?

The control group consists of participants who do not receive the experimental treatment being studied. Instead, they get a placebo (a fake treatment; for example, a sugar pill); a standard, nonexperimental treatment (such as vitamin C, in the zinc study); or no treatment at all, depending on the situation.

How is the treatment/control difference calculated?

The treatment/control difference is given by the estimate of the coefficient "a," and its standard error was used to calculate significance levels. The mean value for the treatment group was calculated as a weighted average of the individual site means for the treatment group.

What is the difference between a control group and treatment?

The control group receives either no treatment, a standard treatment whose effect is already known, or a placebo (a fake treatment). The treatment is any independent variable manipulated by the experimenters, and its exact form depends on the type of research being performed. In a medical trial, it might be a new drug or therapy.

What is the difference between Control Group 1 and 2?

Control group 1 gets an identical-looking sugar pill (a placebo) Control group 2 gets a pill already approved to treat high blood pressure Since the only variable that differs between the three groups is the type of pill, any differences in average blood pressure between the three groups can be credited to the type of pill they received.

Can the control and experimental groups be the same?

Yes it is possible in crossover study. The participants in both groups can act as controll as well as experimental subjects. Mam in our field of orthodontics, we have split mouth design studies in which both control n experimental subjects are the same.

Is control treatment the same as control group?

An experimental group, also known as a treatment group, receives the treatment whose effect researchers wish to study, whereas a control group does not. They should be identical in all other ways.

Are the treatment and control groups balanced?

In a controlled, randomized experiment, treatment and control groups should be roughly the same — balanced — in their distribution of pre-treatment variables. But how nearly so? Reports of clinical trials are urged to present tables of treatment and control group means of x-variables (Campbell et al.

How are treatment control and placebo groups different from each other?

A control group may receive a placebo or they may receive no treatment at all. A placebo is something that appears to the participants to be an active treatment, but does not actually contain the active treatment.

Can you have two control groups?

The possibility of using more than one control group has often been briefly mentioned in general discussions of observational studies, and many observational studies have used two control groups.

How does the control group setup in an experiment differ from the other setups in the same experiment?

The control group and experimental group are compared against each other in an experiment. The only difference between the two groups is that the independent variable is changed in the experimental group. The independent variable is "controlled" or held constant in the control group.

Does the control group have to be the same size?

The size of the control group, or any test group for that matter, depends on the size of the total population. If the experiment is run on a population size of only 100 participants, a 5% control group would be only 5 individuals, which would certainly diminish the significance of the results.

How do experimental and control groups differ explain with the help of an example?

Experimental groups differ from control groups as independent variable manipulation occurs in an experimental group whereas it is absent in a control group. For example, in a study conducted by Latane and Darley, there were two experimental groups and one control group.

Does randomization create comparable treatment and control groups?

Randomization as a method of experimental control has been extensively used in human clinical trials and other biological experiments. It prevents the selection bias and insures against the accidental bias. It produces the comparable groups and eliminates the source of bias in treatment assignments.

Why Some studies include both a control group and a placebo treatment?

Both placebos and controls are used in research studies to prevent the placebo effect, or the real or apparent improvement in a patient's condition due to wishful thinking by the investigator or the patient.

What is meant by blinding and double blinding?

In medical trials, the term blinding, or double-blind, usually refers to the practice of keeping patients in the dark as to whether they are receiving a placebo or not. It can also refer to allocation concealment, which is used to avoid selection bias.

Why do experiments use a control group and treatment group?

A typical use of a control group is in an experiment in which the effect of a treatment is unknown and comparisons between the control group and the experimental group are used to measure the effect of the treatment.

What is cross validated?

Cross Validated is a question and answer site for people interested in statistics, machine learning, data analysis, data mining, and data visualization. It only takes a minute to sign up.

Is TREAT1 a Cgroup?

To code 3 exposure levels, you need two contrasts. TREAT1 is a comparisonal group, but TREAT2 is also listed as a cgroup. Thus assuming TREAT1 and TREAT2 is for low and high exposure, the control is the reference.

Can you fit homoscedasticity in one model?

You can fit it in one model if the homoscedasticity assumption holds or other adjustments are made

Why is it important to compare treatment and control groups?

The comparability of the treatment and control groups at randomization is also important because it is the first stage in our investigation of a set of methodological problems that could result in biased estimates of channeling's impact. Differences between treatment and control groups in the types of individuals who fail to respond to interviews could result in noncomparable groups in the sample being analyzed, even if the full samples were comparable. Differences in the way baseline data were collected for treatments and controls could lead to differential measurement error, which could cause regression estimates of program impacts to -be biased. In order to assess these other potential sources of bias, it is important to first determine whether the two groups were comparable before the baseline interview.

How are treatments different from controls?

Demographics and living arrangements show no significant differences between treatments and controls for the financial control model. Slightly more treatments than controls are male; slightly more controls than treatments are black. The proportion of treatments with income in excess of 1,000 dollars per month was significantly lower for treatments than controls (5.7 versus 7.3 percent, respectively); however, the difference is not large in absolute terms and the average incomes of the two groups do not differ significantly. Just over 2 percent of both treatments and controls lived in long term care institutions at the time the screen.

What are the factors that lead to differences in the mean values of the pre-application characteristics of the treatment and control groups?

Only two factors can lead to differences in the true mean values of the pre-application characteristics of the treatment and control groups: deviation from the randomization procedures and normal sampling variability. Deviations from the carefully developed randomization procedures could be either deliberate (e.g., site staff purposely misrecording as treatments some applicants who are randomly assigned to the control group, but who have especially pressing needs for assistance) or accidental (e.g., misrecording of a sample member's status). The dedication and professionalism of this site staff and the safeguards built into the assignment procedure make either occurrence very unlikely. Site staff were extremely cooperative in faithfully executing the procedures. Sampling variability, on the other hand, is the difference between the two groups that occurs simply by chance. For the sample sizes available at the model level, such differences between the two groups should be very small, and statistically insignificant.

Why was the screening instrument used in the Channeling project?

The screening instrument was designed for a short telephone interview, to be administered in a uniform manner by each of the 10 demonstration projects. The telephone screening process was intended to reduce the cost of determining appropriateness for channeling compared to using a comprehensive in-person assessment for that purpose. Channeling project staff who conducted the screening interviews were in a separate administrative unit from assessment and case management staff. This was required chiefly to preserve the integrity of the experimental design--the potential for influencing the behavior of persons assigned to the control groups through contact with channeling staff was minimized by this administrative separation.

Why is treatment/control difference statistically tested?

However, because of the relatively small number of observations at each site, most of the analysis of channeling will be based on treatment/control differences at the model level, to ensure a high level of precision (i.e., the ability to distinguish between fairly small impacts of channeling and differences between treatment and control groups arising simply by chance).

How many statistically significant differences are there between treatments and controls?

Out of over 250 comparisons at the five basic sites, we find 15 statistically significant differences between treatments and controls. (at the 90 percent or greater confidence level). This is substantially less than the 25 that might be expected to occur simply by chance. As shown in Table 4, the significant differences were more prevalent in Kentucky than in other sites, but tended to be scattered rather than concentrated in specific variables. Thus, there is no indication of systematic tampering with the random assignment process.

Is there a difference between treatment and control?

There is very little difference between treatments and controls in the basic case management model. Of the 53 variables examined in Table 3, the only statistically significant difference between treatments and controls was in the proportion of referrals from case management agencies. Treatment/control differences tended to be small in relation to the mean for the treatment group, with very low test statistics. Furthermore, a joint test that the multiple correlation' between treatment/control status and all of the variables (controlling for site) is zero could not be rejected. 11

Is adjustment for pretreatment differences a desperate strategy?

I disagree! Adjusting for pre-treatment differences is not a “desperate” strategy. It’s standard statistics (for example in chapter 19 of Regression and Other Stories, but it’s an old, old method; we didn’t come up with it, I’m just referring to our book as a textbook presentation of this standard method), nothing desperate at all. Also, no need to “wring significance” out of anything. The point is to summarize the evidence in the study. The adjusted analysis should indeed “move our needle” to the extent that it resolves concerns about imbalance. In this case the data are simple enough that you could just show a table of outcomes for each category treatment or control and high or low blood pressure. I guess I’d prefer to use blood pressure as a continuous predictor but that’s probably not such a big deal here.

Is the pre-existing group difference in blood pressure dramatic?

Although the pre-existing group difference in blood pressure was dramatic, their results were several orders of magnitude more dramatic. The paper Pachter is criticizing does a regression to determine whether the results are still significant even controlling for blood pressure, and finds that they are. I can’t see any problem with their math, but it should be remembered that this is a pretty desperate attempt to wring significance out of a small study, and it shouldn’t move our needle by very much either way.

Did the randomization of the study in Cordoba Hospital have malfeasance?

Or to put it another way – perhaps correcting for multiple comparisons proves that nobody screwed up the randomization of this study; there wasn’t malfeasance involved. But that’s only of interest to the Cordoba Hospital HR department when deciding whether to fire the investigators. If you care about whether Vitamin D treats COVID-19, it matters a lot that the competently randomized, non-screwed up study still coincidentally happened to end up with a big difference between the two groups. It could have caused the difference in outcome.

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How to do one way ANOVA?

1. Run just a one-way ANOVA, dropping the covariate. But do this only if really, truly, the only thing you’re interested in is whether these experimental conditions show differences in satisfaction, regardless of age. The one-way ANOVA will reflect the effects of the treatment groups, regardless of age.

What is the p-value of age and experimental group?

The p-value for the interaction between age and experimental group was .011. Quite significant.

Control Groups in Experiments

  • Control groups are essential to experimental design. When researchers are interested in the impact of a new treatment, they randomly divide their study participants into at least two groups: 1. The treatment group (also called the experimental group) receives the treatment whose effect the researcher is interested in. 2. The control groupreceives either no treatment, a standard treat…
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Control Groups in Non-Experimental Research

  • Although control groups are more common in experimental research, they can be used in other types of research too. Researchers generally rely on non-experimental control groups in two cases: quasi-experimental or matching design.
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Importance of Control Groups

  • Control groups help ensure the internal validityof your research. You might see a difference over time in your dependent variable in your treatment group. However, without a control group, it is difficult to know whether the change has arisen from the treatment. It is possible that the change is due to some other variables. If you use a control gro...
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