[PDF] Top 20 Psychological advocacy toward healing (PATH): study protocol for a randomized controlled trial

... The aims of the qualitative analysis will be twofold: first to understand the meaning and perceived effectiveness of the intervention in the context of the women’s lives, and second to deepen our understanding of the ... See full document

... Repeated and early exposure to stress, above all in per- sons with a particular genetic disposition, as well as high level of trait anxiety, may result in a decreased threshold for developing anxiety [6-8]. ... See full document

... This protocol describes a cluster randomized controlled trial aimed at evaluating an 8-session integrated psychological and advocacy intervention (Nguvu) with female adult ... See full document

... Though most trauma survivors recover with time, for some, posttraumatic stress symptoms due to war experi- ences in childhood show persistence for years and even decades [6, 7], and have been shown to be related to a ... See full document

... There is much research evidence available to guide the management of SWHSI; however, as NICE reflected in their 2012 guidelines [3], there is a need for robust, experimental evidence to assess the most clinical and ... See full document

... parents’ psychological functioning, their parental behavior, and the parent-child relationship ...present study aims to test the relative efficacy of two components added to TF- CBT focussing on ... See full document

... in randomized trials of total omega-3 long chain polyunsaturated fatty acid (LCPUFA) supplementation ...US trial conducted by the NICHD Maternal Fetal Network trial ob- served no decrease in ePTB ... See full document

... Contemporaneous notes will be made during each interview and uploaded to NVivo analytical software be- fore thematic analysis [45]. To generate an initial coding framework, an independent thematic analysis will be ... See full document

... same protocol as the first, with additional questions relating to volunteering experiences in the intervention ...2 Psychological measures used in the ... See full document

... The protocol described in this paper is of a pragmatic randomized controlled trial comparing eight sessions of telephone CBT to an active social control, referred to as ...face-to-face ... See full document

... this trial is limited, there are clearly predefined safety limits of PSH incidence and complications to determine when to prematurely finish the trial as unethical to con- ...the trial is designed to ... See full document

... This protocol paper outlines the background and design of a randomized controlled trial of Baby Triple P for first-time pregnant parents in high-risk ...this study will be the re- ... See full document

... whom study drug cannot be started within 48 hours after evacuation of the hematoma; 12) patients for whom it is known at the time of screening that certain follow-up, protocol-mandated imaging assess- ments ... See full document

... no randomized controlled trials (RCTs) have been ...a protocol for an RCT comparing a standard suture closure to mesh reinforcement with biological intra-abdominal mesh after stoma closure ... See full document

... The study has been approved by the Institutional Review Broad of the University of Hong Kong/Hospital Authority Hong Kong West Cluster and has been registered under Clinical Trials Registry (trial number ... See full document

... Bi-TPAI trial is a national, multicenter, parallel group, open, non-inferiority, randomized controlled trial that will include 220 patients with HTG-AP, from 17 large tertiary hospitals in ... See full document

... The study visits will be per- formed by investigators who are not involved in the surgi- cal ...a study nurse will be in charge of changing the wound dressing and will not be involved further in the ... See full document

... All data will be collected in personal CRFs, which will be stored in the patient’s own hospital. Copies of the completed forms will be sent to our coordinating center (Canisius-Wilhelmina Hospital, Nijmegen). All data ... See full document

... The rates for the primary endpoint: major morbidity, re- intervention and mortality for PC were 6.2, 13.1 and 12.7% respectively in the review and 22.2, 18.5 and 14.8% in our own series. We believe that the 6.2% ... See full document

... Aligned with the overall study aims, there are two main hy- potheses for which data analyses of the phase 2 RCT are planned. Hypothesis 1 (primary outcome) is that perinatal patient participants with depressive ... See full document