Introduction to Crossover Randomized

Crossover randomized controlled trials (RCT) assessing the effects of oral caffeine intake on several aspects of performance in female TSA were selected.

Methods: This study was a crossover randomized clinical trial.

Methods Ten individuals (mean age: 63 ± 9 years) with unilateral transfemoral amputation due to vascular conditions designated as MFCL K2 participated in this longitudinal crossover randomized clinical trial.

METHOD AND MATERIALS A crossover randomized controlled clinical trial included 36 children aged 3 to 5 years, rated I or II according to the Frankl scale and ASA I or II.

Results: Thirty-one research studies were included: 11 experimental (including four crossover randomized controlled trials), three pre-post design, 13 observational (12 cross-sectional, one longitudinal), and four qualitative.

Materials and Method: In this crossover randomized clinical trial, 30 participants were selected using convenience sampling method.

Methods This crossover randomized controlled trial had four periods.

Methods We searched seven databases for randomized controlled trials (RCTs) and crossover randomized trials of KT in DOMS, from the earliest date available to December 31, 2019.

A mixed-methods approach was used to gather information on the impact of four FOP-NL schemes on consumers’ selection of food products according to the perception of their nutritional quality, combining a systematic literature review, focus groups (FG), in-depth individual interviews, and an open-label crossover randomized controlled study.

The purpose of this double-blinded, crossover randomized, and counterbalanced study was to compare effects of ingesting a tepid commercially available carbohydrate-menthol containing sports drink (Menthol) and an isocaloric carbohydrate-containing sports drink (Placebo) on thermal perception and cycling endurance capacity "in a simulated home virtual cycling environment".

Parallel or crossover randomized controlled trials that addressed the effectiveness of rTMS in patients with stroke, published from inception to November 28, 2019, were included.

In this crossover randomized double-blind placebo-controlled study, we investigated the effects of an analgesic treatment on the presence of nociception-related behaviors.

We will include parallel-design and crossover randomized clinical trials that has adult Black people with essential hypertension as the population.

In this single-center crossover randomized controlled trial in healthy volunteers, subjects were randomized to receive arterial occlusion to the left arm and venous stasis on the right arm (n = 5) or vice versa (n = 5) during 5 min.

METHODS Post-hoc analyzes of HeadPoST, a pragmatic cluster-crossover randomized trial of lying flat versus sitting up head positioning in 11,093 patients (age ≥18 years) with acute stroke at 114 hospitals in 9 countries during 2015-2016.

In the first crossover randomized controlled trial, we compared the short-term effects induced by shooting and puzzle video-games in visual perception, sensorimotor and reading skills in children with developmental coordination disorder and dyslexia.

Methods: We performed a crossover randomized controlled trial.

This pilot study will use a crossover randomized controlled design.

Materials and methods A 3-arm, crossover randomized controlled trial included 30 children of age 9–12 years requiring extraction of primary maxillary posterior teeth.

Methods This was a crossover randomized controlled trial.

Eligible randomized controlled trials of auricular acupressure in treating CINV were collected, including crossover randomized design study.

One placebo-controlled crossover randomized trial assessed the role of baclofen in 60 female patients with dysfunctional voiding.

The entire study was conducted as a single-dose crossover randomized bioequivalence study with open-label, two treatment, two-period, and two sequences on 24 healthy volunteers under fasting condition.

Objective: The purpose of this study was to examine the effect of PA-EST on the upper limb motor function in a crossover randomized controlled trial.

Method: Twenty-one children with DLD (ages 5;9–6;9 [years;months]) were included in a crossover randomized controlled trial (intervention, n = 10; waiting control, n = 11).

A 2-arm pilot crossover randomized controlled trial is being performed.

To address this question, we have undertaken the STOP Sugars NOW trial (NCT03543644), a pragmatic “head-to-head” crossover randomized controlled trial of the effect of NSBs (the intended substitution) versus water (the standard of care) as a replacement strategy for SSBs on glucose tolerance and gut microbiome diversity.

A Comparative Crossover Randomized Study of Miller and Macintosh Blade for Laryngoscopic View and Ease of Intubating Conditions in Adults.

METHODS We determined the strategies for fulfillment of EFIC requirements at five regional coordinating centers of the Pragmatic Airway Resuscitation Trial (PART), a cluster-crossover randomized trial comparing airway devices in out-of-hospital cardiac arrest.

The Head Positioning in Acute Stroke Trial (HeadPoST) is a pragmatic, international, cluster crossover randomized trial of 11,093 patients with acute stroke assigned to a lying-flat (0°) or sitting-up (head elevated ≥30°) position.

STUDY DESIGN Prospective crossover randomized study.

Methods We performed a crossover randomized controlled trial of the WISCA tool between July 1, 2015 and June 30, 2018 at 4 hospitals.

PURPOSE The purpose of this crossover randomized clinical trial was to assess the effectiveness of various chemical hygiene clinical protocols in reducing the microbial viability of biofilm formed on complete dentures.

During robotic surgical stages, 2 crossover randomized groups (conditions) of neuromuscular relaxation were studied: Moderate (1 twitch in the train-of-four stimulation) and Deep (1-2 twitches in the posttetanic count).

METHOD This is a crossover randomized controlled trial.

Methods We conducted a blinded, crossover randomized trial among MSM and MSW in Atlanta, Georgia, USA.

Material and Methods Both healthy volunteers (n= 80) and patients (n= 100) were enrolled in this crossover randomized study.

Methods: A crossover randomized study was performed on 12 healthy volunteers receiving a single dose of regular ibuprofen tablet (200 mg) and enteric-coated capsule (200 mg).

Method: a longitudinal, prospective, interventional, crossover randomized study, with a quantitative approach and before-and-after type, with a population composed of 120 nursing students distributed randomly between experimental and control group.

METHODS In a double-blind crossover randomized controlled trial, 13 prediabetic adults (37.

Single-site double-blind crossover randomized controlled trial.

This crossover randomized clinical trial assesses clinical success and marginal bone resorption of dental implants bearing a surface molecular layer of covalently-linked hyaluronan in comparison with control implants up to 36 months after loading.

Effects of Combined Tracheal Suctioning and Expiratory Pause: A Crossover Randomized Clinical Trial.

Methods: This was a crossover randomized controlled trial that was conducted on 40 obese or overweight clerical staff of the university.

Results: the 14 papers included reported different study designs; 2 studies were open-label, 9 were crossover randomized clinical trials (RCTs), and 3 were parallel group RCTs.

Methods Using a crossover randomized design, 92 adults with type 1 or 2 diabetes tested two Android apps (mySugr and OnTrack) for seven tasks including data entry, blood glucose (BG) reporting, and data sharing.

Our study utilized a repeated-measures crossover randomized design and captured measures of stress and well-being whilst participants walked in each condition (n=23).

Results: Nineteen studies were included in this review: 15 randomized, 1 quasi-randomized, and 3 crossover randomized controlled trials.

Settings and Design: In a triple-blind crossover randomized trial, 44 healthy volunteers (21–25 year old) were recruited according to the inclusion criteria and were randomly allocated into two groups (22 each).

In a crossover randomized study, 11 men (age = 62.

A crossover randomized controlled trial—for six months—was conducted.

Methods: This was a crossover randomized study involving 10 patients.

Design, Setting and Participants Cluster-crossover randomized clinical trial involving patients, family members, and clinicians from 36 adult ICUs with restricted visiting hours (<4.