Satisfaction Measurement of Publics with Bicycle Path

Import 05/08/2014Má bakalářská práce se zabývá problematikou měření spokojenosti veřejnosti s cyklostezkami. Cílem mé bakalářské práce bylo zjistit a následně vyhodnotit spokojenost veřejnosti s cyklistickými trasami v Ostravě a okolí. Výzkum byl proveden pomocí dotazníkového šetření. V závěru mé bakalářské práce jsou navrhnuty návrhy a doporučení pro zvýšení spokojenosti veřejnosti s cyklistickými trasami.My thesis deals with the satisfaction measurement of publics with bicycle path. The goal of my thesis was to find and evaluate satisfaction measurement of publics with bicycle path in Ostrava and around. Research was performed through questionnaire survey. In the end my thesis are designed proposals and recommendations to improve satisfaction of publics with bicycle path.116 - Katedra marketingu a obchoduvelmi dobř

From protocol to published report:a study of consistency in the reporting of academic drug trials

BACKGROUND: Unacknowledged inconsistencies in the reporting of clinical trials undermine the validity of the results of the trials. Little is known about inconsistency in the reporting of academic clinical drug trials. Therefore, we investigated the prevalence of consistency between protocols and published reports of academic clinical drug trials. METHODS: A comparison was made between study protocols and their corresponding published reports. We assessed the overall consistency, which was defined as the absence of discrepancy regarding study type (categorized as either exploratory or confirmatory), primary objective, primary endpoint, and – for confirmatory trials only – hypothesis and sample size calculation. We used logistic regression, χ(2), and Fisher’s exact test. RESULTS: A total of 282 applications of academic clinical drug trials were submitted to the Danish Health and Medicines Authority in 1999, 2001, and 2003, 95 of which fulfilled the eligibility criteria and had at least one corresponding published report reporting data on trial subjects. Overall consistency was observed in 39 % of the trials (95 % CI: 29 to 49 %). Randomized controlled trials (RCTs) constituted 72 % (95 % CI: 63 to 81 %) of the sample, and 87 % (95 % CI: 80 to 94 %) of the trials were hospital based. CONCLUSIONS: Overall consistency between protocols and their corresponding published reports was low. Motivators for the inconsistencies are unknown but do not seem restricted to economic incentives

Characteristics of included academic drug trials by publication status.

<p>Characteristics of included academic drug trials by publication status.</p

Time from approval to publication of completed academic drug randomized controlled trials (RCTs) and non-randomized controlled trials (non-RCTs).

<p>Time from approval to publication of completed academic drug randomized controlled trials (RCTs) and non-randomized controlled trials (non-RCTs).</p

Effect of European Clinical Trials Directive on academic drug trials in Denmark: retrospective study of applications to the Danish Medicines Agency 1993-2006

Objective To determine the impact of the European Union’s Clinical Trials Directive on the number of academic drug trials carried out in Denmark

Reasons for non-initiation, non-completion, and non-publication of academic drug trials.

<p>Reasons for non-initiation, non-completion, and non-publication of academic drug trials.</p

Time from approval to publication of completed academic drug trials.

<p>(n = 114).</p

Number and proportion of initiated, completed, and published academic drug trials by year of approval of clinical trial application.

<p>Number and proportion of initiated, completed, and published academic drug trials by year of approval of clinical trial application.</p