Sample size: how many participants are needed in a trial?

نویسنده

  • Philip Sedgwick
چکیده

Researchers investigated the effectiveness of a home based early intervention on children’s bodymass index (BMI) at age 2 years. A randomised controlled superiority trial was used. The intervention consisted of eight home visits from specially trained community nurses in the first 24 months after birth; this was in addition to the usual childhood nursing service from community health service nurses. The control group received the usual childhood nursing service alone. Participants were first time mothers and their infants. The primary outcome was children’s BMI at age 2. The sample size calculation was based on having 80% power to detect a difference in mean BMI of 0.25 units between treatment groups at age 2, using a two sided hypothesis test and critical level of significance of 0.05. It was assumed that the standard deviation of observations in each group was the same and equal to 1.5 BMI units. A total sample size of 504 participants (252 in each treatment arm) was required. To allow for an estimated 20% dropout rate it would be necessary to recruit 630 first time mothers. In total, 667 first time mothers and their infants were recruited to the trial. At age 2 years, mean BMI was significantly lower in the intervention group compared with the control group (16.53 v 16.82; difference 0.29, 95% confidence interval −0.55 to −0.02; P=0.04). The researchers concluded that a home based early intervention delivered by trained community nurses was effective in reducing mean BMI in children at age 2 years. Which of the following statements, if any, are true? a) A difference in mean BMI of 0.25 between treatments was the smallest effect of clinical interest

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Determination of the Size of a Trial, Using Lindley’s Method

Extended Abstract. When a new treatment is being considered, trials are carried out to estimate the increase in performance which is likely to result if the new treatment were to replace the treatment in current use. Many authors have looked at this problem and many procedures have been introduced to solve it. An important feature of the analysis in this work is that account is taken of the fac...

متن کامل

An Introduction to the Field Trials Methodology

  The knowledge related to the methodology of the field trial study as a type of intervention studies, yet for many of our researchers is not fully understood. The aim of the current study was a better understanding of conducting this type of research. Field trial studies are done on healthy individuals and aim to prevent. These types of studies such as clinical trials are performed on both i...

متن کامل

تعیین حجم نمونه در داده های دوتایی برای دو گروه مستقل در مطالعات پزشکی

Backgound and Objectives: Nowadats, it is very common to investigate the effect of a new method or medicine by using a comparison between two independent groups in many clinical studies, but unfortunately the sample size part has not been done based on scientific formulas but on practical issues in some researches of this type of cinical studies, and this makes some unreliable results. Therefor...

متن کامل

Sample size calculation in clinical trials: part 13 of a series on evaluation of scientific publications.

BACKGROUND In this article, we discuss the purpose of sample size calculation in clinical trials, the need for it, and the methods by which it is accomplished. Study samples that are either too small or too large are unacceptable, for clinical, methodological, and ethical reasons. The physicians participating in clinical trials should be directly involved in sample size planning, because their ...

متن کامل

An audit of sample sizes for pilot and feasibility trials being undertaken in the United Kingdom registered in the United Kingdom Clinical Research Network database

BACKGROUND There is little published guidance as to the sample size required for a pilot or feasibility trial despite the fact that a sample size justification is a key element in the design of a trial. A sample size justification should give the minimum number of participants needed in order to meet the objectives of the trial. This paper seeks to describe the target sample sizes set for pilot...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • BMJ

دوره 346  شماره 

صفحات  -

تاریخ انتشار 2013