Kramer, M. S., et al., & Promotion of Breastfeeding Intervention
Trial Study Group.
Not exact matches
We chose to model the effects on body weight because good evidence (from both
trials and epidemiological
studies) links regular consumption of sugar sweetened drinks to weight gain.8 10 12 Moreover, data from longitudinal
studies support the idea that changes in the price of sugar sweetened drinks are linked to changes in body weight.20 Other
groups have used this form of modelling to estimate the effects of a sugar sweetened drink tax on obesity.18 21 22
The result of the
study showed that a significant amount more women in the
study group went into labor when compared with the control
group in each of the three
trials.
COMET
Study Group UK, «Effect of Low - Dose Mobile versus Traditional Epidural Techniques on Mode of Delivery: A Randomised Controlled
Trial,» Lancet 358, no. 9275 (2001): 19 — 23.
One randomized controlled
trial comparing home - visited families with control participants who received other community services found a statistically significant difference in mean depressive symptoms at two years post-enrollment, but this contrast was nonsignificant at three years post - enrollment.15 A second
study of Early Head Start found no differences in depressive symptoms between intervention and control
group participants post-intervention, although a difference was detected at a longer - term follow - up prior to children's enrollment in kindergarten.10 Other randomized controlled
trial studies have not found effects of home visitation on maternal depressive symptoms.12, 16,17
A series of randomized control
trials of a nurse home visitation program show a range of positive effects on maternal health, including decreases in prenatal cigarette smoking, fewer hypertensive disorders in pregnancy, and fewer closely spaced subsequent pregnancies., A randomized control
study of another program that works with a particularly high - risk population found that participant mothers showed significantly lower depressive symptoms than those in the control
group and were less likely to report feeling stressed a year after participation.
Controlled clinical
trials and observational
studies including an internal comparison
group
24 randomised and 2 non-randomised
trials of intervention packages, including mainly: building community - support or women's
groups (9
studies), community mobilisation and antenatal and postnatal home visitation (7
studies), community mobilisation and home - based neonatal treatment (1
study), training traditional birth attendants who made antenatal and intrapartum home visits (2
studies), home - based neonatal care and treatment (2
studies), and education of mothers and antenatal and postnatal visitation (2
studies)
This
study is a randomized clinical
trial (RCT) with 50 mother / infant pairs in the intervention arm, 50 in one control
group and 25 in a third control
group.
In addition, there was no effect on breastfeeding duration when the pacifier was introduced at 1 month of age.280 A more recent systematic review found that the highest level of evidence (ie, from clinical
trials) does not support an adverse relationship between pacifier use and breastfeeding duration or exclusivity.281 The association between shortened duration of breastfeeding and pacifier use in observational
studies likely reflects a number of complex factors such as breastfeeding difficulties or intent to wean.281 A large multicenter, randomized controlled
trial of 1021 mothers who were highly motivated to breastfeed were assigned to 2
groups: mothers advised to offer a pacifier after 15 days and mothers advised not to offer a pacifier.
We searched the Cochrane Pregnancy and Childbirth
Group's
Trials Register (28 January 2013) and reference lists of retrieved
studies.
The M@NGO
Study (Midwives at New
Group practice Options): A randomised controlled
trial of caseload midwifery care.
Corruption
Trials and Two Reform Reports Make the Case for Action Now In light of the corruption trials of two former legislative leaders taking place this week and New York State's D - minus grade in how it handles issues of integrity from a national comparison study, New York's leading good government groups today called upon the -LS
Trials and Two Reform Reports Make the Case for Action Now In light of the corruption
trials of two former legislative leaders taking place this week and New York State's D - minus grade in how it handles issues of integrity from a national comparison study, New York's leading good government groups today called upon the -LS
trials of two former legislative leaders taking place this week and New York State's D - minus grade in how it handles issues of integrity from a national comparison
study, New York's leading good government
groups today called upon the -LSB-...]
In light of the corruption
trials of two former legislative leaders taking place this week and New York State's D - minus grade in how it handles issues of integrity from a national comparison
study, New York's leading good government
groups today called upon the New York State legislature and governor to complete the job of reforming our laws governing public ethics.
Mr. Silver's
trial is a case
study in everything good government
groups want to change.
One of the best ways scientists have to prove cause and effect in medicine is to conduct a randomized controlled
trial, in which
study subjects are randomly assigned to two
groups.
One of the limitations of the
study was that the component of the
trial that
studied which students sought help for depression did not have a control
group.
Promising results from the new
trial would be a major step forward for a field that has long been criticized for
studies that are poorly designed, incomplete or lack control -
group comparisons, as well as for the peddling of unproved therapies in many clinics worldwide.
Both adverse outcomes need to be
studied further, according to Legro, who led a team that hosted the Chinese collaborators at Penn State College of Medicine for five weeks as the
group wrote the protocol for the multi-center
trial and participated in regular steering committee meetings overseeing the
trial.
Another problem is that modeling
studies, like this one, are inherently less powerful than other kinds of medical research: randomized clinical
trials, the gold standard in medical research, in which patients are randomly assigned different treatments or no treatment; case - control
studies, which compare patients who have a condition with those who do not; or cohort
studies, which determine the risk of contracting a disease by
studying a
group of people with similar demographics.
The actual disparity in number of cases between the two
groups was small, with 129 lung cancers in all, and the
trial wasn't set up to
study that disease.
Wyss - Coray, whose
group did most of the mouse
studies that inspired the clinical
trial, now plans to conduct a second, larger
trial using plasma from which many proteins and other molecules have been removed.
The
study is similar to a clinical
trial the Mahidol
group recently completed along the Thai / Myanmar border.
We urge the adoption of policies that ensure opportunities for people to participate in research
studies and clinical
trials without fear that the information generated by their participation will be inappropriately disclosed and adversely affect their health insurance status or that of their families, either as individuals or as members of a particular
group.
The new
study is a meta - analysis of three randomized controlled
trials conducted by the Alliance for Clinical Trials in Oncology (formerly Cancer and Leukemia Group B)(CALGB) with support from the NCI, Intergroupe Francophone du Myélome (IFM), and the Gruppo Italiano Malattie Ematologiche dell «Adulto (GI
trials conducted by the Alliance for Clinical
Trials in Oncology (formerly Cancer and Leukemia Group B)(CALGB) with support from the NCI, Intergroupe Francophone du Myélome (IFM), and the Gruppo Italiano Malattie Ematologiche dell «Adulto (GI
Trials in Oncology (formerly Cancer and Leukemia
Group B)(CALGB) with support from the NCI, Intergroupe Francophone du Myélome (IFM), and the Gruppo Italiano Malattie Ematologiche dell «Adulto (GIMEMA).
A second
study showed that training in realistic environments, including practiced encounters with armed - opponent actors in buildings and streets, improved their shooting accuracy under stress Similarly,
trials with 66 of the officers revealed that those who trained weekly on their own in a combat sport such as karate or kickboxing performed better under high - anxiety fights than those with no additional training, although both
groups suffered performance decreases when conditions shifted from low to high anxiety.
Although epidemiological
studies have suggested that moderate drinking can lower a person's risk of heart attack or stroke, that possibility has not been
studied in a randomized
trial with a control
group.
Principal investigator E. Shelley Hwang, M.D., chief of breast surgery at the Duke Cancer Institute and vice chair of research in the Duke University Department of Surgery, will lead the
study through the cooperative
group, The Alliance for Clinical
Trials in Oncology.
Often clinical
studies fall short of the rigorous methodology demanded by «gold standard» clinical
trials, in which patients are assigned to treatment
groups at random and nobody knows which
group is which.
«However, as immunosuppression drugs required for transplantation can have significant adverse side effects, the treatment only makes sense for people who have frequent severe hypoglycemia despite optimal diabetes management, or for those already on immunosuppressant drugs for a kidney transplant, a
group being
studied in another Phase 3
trial.»
CT - P13 has previously demonstrated pharmacokinetic (PK) equivalence to INX in the PLANETAS
trial, a randomised double - blind, parallel
group study of 250 patients with AS, and was recently approved by the European Medicines Agency.
The results of the
trial — a combined phase 1 and 2
study — strongly support testing of the drug in a larger
group of patients in both phase 2 and 3
trials, the authors say.
The
study demonstrated that a
group of
trial participants with low 21 - gene recurrence score (Oncotype DX ® Recurrence Score ®) results of 10 or less who received hormonal therapy alone without chemotherapy had less than a one percent chance of distant recurrence at five years.
«Our population in this
trial also had a high response rate in the control
group, so further
studies are needed in broader populations to assess the efficacy of buprenorphine implants versus sublingual buprenorphine in other settings.»
To address that debate, Kojic's
study, dubbed «AIDS Clinical
Trials Group Protocol 5240,» measured the safety and immune system response of the vaccine in HIV - positive women aged 13 to 45 with a wide range of immune statuses.
Julia Lewis, MD (Vanderbilt University School of Medicine) and her colleagues in the Collaborative
Study Group conducted a 441 - patient randomized clinical
trial to test the potential of a compound called ferric citrate to bind phosphorus, increase iron stores, and reduce the usage of IV iron and ESAs.
Although the
study began as a randomized
trial that divided subjects into four treatment
groups (placebo, deprenyl, α - tocopherol, and deprenyl / α - tocopherol), this was terminated early because positive effects of deprenyl were observed and all subjects then received deprenyl for approximately 18 months.
The authors, who are now planning to begin clinical
trials based on this
study, state that the three enzymes can be promising therapeutic targets for a diverse and broad
group of DLBCL patients.
Contrary to the proclamations of many scientists, unreliable medical
study results do not disappear with large, randomized controlled
trials, in which subjects are randomly assigned to a treatment or placebo
group.
Hypertension is the most important treatable risk factor for cardiovascular disease, and while it is especially common in the elderly and in patients with chronic kidney disease (CKD), these are the least
studied groups in randomized controlled
trials examining the health effects of lowering blood pressure.
The
study, published in the July issue of the journal Epidemiology, offers benefits over typically used randomized clinical
trials, as such
studies are often too small to identify rare side effects or may be performed in a
group of patients who do not take other types of medications or have other conditions that could skew the drug's effect in a broader
group following approval.
The
study — conducted by the Clinical Investigator Collaborative, a multi-centre, Phase II clinical
trials group supported by the Allergy, Genes and Environment Network (AllerGen)-- recruited 31 patients over five sites across Canada.
The
study was the first randomized - controlled
trial to examine the potential benefits of the low fat diet on the management of MS.. The
study found no significant differences between the two
groups in brain lesions detected on MRI brain scans or on other measures of MS.. But while the number of
trial participants was relatively small,
study leaders believe the significantly improved fatigue symptoms merited further and larger
studies of the diet.
The series started in 2009, when the U.S. government funded a team of researchers to recruit and
study participants for the Testosterone
Trial — a
group of seven long - term
studies of how testosterone therapy affects sexual activity, energy level, memory, heart and bone health, and the ability to walk a certain distance.
Their most powerful tool in this job is the randomized controlled
trial, a type of experiment in which researchers separate participants into two or more
groups and subject some of them to the intervention to be
studied, like a new drug or surgical procedure.
For this
study, the Swiss researchers pooled data with two other
groups that conducted Phase 1
trials of the vaccine in Africa — in Lambaréné, Gabon, and Kilifi, Kenya.
Maria Carrillo, vice president of medical and scientific relations at the Alzheimer's Association, an advocacy
group, applauds NIH's giving the
trial a green light: Targeting the APOE4 population will «increase the possibility that participants in the
trial will become symptomatic during the period of the
study so that the scientists can assess whether the drug intervention is having an impact on delaying or preventing Alzheimer's symptoms, without having to wait 10 or 15 years or more,» she says.
For the
study, Baron performed an analysis of data from a 2010 clinical
trial (by the same
group of Northwestern researchers on the current paper) that demonstrated the ability of aerobic exercise to improve sleep, mood and vitality over a 16 - week period in middle - age - to - older adults with insomnia.
Focus
group studies revealed that older people across Europe feel that they have the right to be invited to clinical
trials, and that they could make the decision to participate themselves.
This is a «drastic» step, says Inder Verma of the Salk Institute for Biological
Studies in La Jolla, California, who headed a special working
group at the National Institutes of Health that investigated the Gelsinger
trial.