Study Characteristics Sample Clauses

Study Characteristics. Study characteristics are summarized in Table 2 (Appendix 2). Five were randomized controlled interventions2, six were feasibility, acceptability studies and six were observational studies. In total, 558 participants with a diagnosis of schizophrenia spectrum disorders and a mean age ranging from 20 to 48 years participated in the 17 studies. 13 studies included individuals with schizophrenia or schizo-affective disorder, one study 2 For clarity, randomized controlled trials are defined as trials with a randomized control group and pre and post outcome measures; Feasibility or acceptability studies are defined as studies that assess the usability, feasibility, and acceptability of an intervention and may have a case control group or single group design; Observational studies are studies where the researcher observes and records behaviour in a systematic way without manipulating variables, e.g. experience sampling methods (Xxxx et al., 2010). included individuals with first episode psychosis, one study included individuals with a dual diagnosis of schizophrenia and substance misuse and two studies included individuals with non-affective psychosis.
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Study Characteristics. Web Based Screening The paper based M-CHAT-R/F is a validated screening tool, where the web-based modality is not currently validated (Xxxxxx et al., 2016). When the M-CHAT was revised in 2014 and combined with the follow-up interview, sensitivity decreased, specificity increased, and PPV increased (Robins et al., 2014). The literature review was not conducted to determine the validity of the M-CHAT-R/F, which has been proven, but to determine if implementing the M- CHAT-R/F with technological assistance would further enhance screening efficiency. Following the American Academy of Pediatrics (AAP) recommendation to screen all children for ASD at their 18 and 24-month well child visits, specialized professionals could not keep up with the increased demand (Wise, Little, Holliman, Wise, & Wang, 2010). The increased demand was not only due to the increase in ASD prevalence, but also due to the number of children being referred for further evaluation following overly sensitive screening (Xxxxxxxx et al., 2015). In order to improve the accuracy of children referred for further evaluation and to reach the number of children needing services, consensus was reached through review that enhancements need to be made to the current processes (Wise et al., 2010).
Study Characteristics. Any request for a Member Region Economic Study should focus on evaluating high-level metrics depicting various possible future scenarios of expanding the power system and quantifying the advantages and disadvantages associated with each scenario. A Member Region Economic Study will not assess the performance of individual assets. A Member Region Economic Study will be documented in a stand-alone report that is separate from the Regional Transmission Plan. Requests for a Member Region Economic Study shall be submitted and considered as follows:
Study Characteristics. The characteristics of the included articles are summarized in Table 1. The 24 eligible studies included 4789 patients with 5163 hepatic observations. One study was prospective,20 whereas the other studies were retrospective. Three studies exclusively included patients with cirrhosis.5, 9, 32 The dominant etiology of liver disease was hepatitis B virus in all but two studies, of which alcoholic liver disease was the dominant etiology in one9 and hepatitis C virus in the other.6 Twelve studies reported proportions of other malignancy such as CCA or cHCC-CCA that exceeded 10% of total observations.5-9, 11, 12, 20, 21, 25, 30, 34 Twelve studies utilized only 3.0-T MRI scanners.8, 11, 12, 20, 21, 23-25, 27, 31, 33, 34 Eighteen studies employed only HBA including gadoxetate or gadobenate dimeglumine as the MRI contrast agent.5, 7, 9-13, 20, 21, 23, 26-29, 31-34 In all studies, CT/MRI interpretation was conducted by multiple image readers, with three or more readers participating in two studies.11, 22
Study Characteristics. A total of 2,871 participants were included, and study sample sizes ranged from one to 370 (Mean = 111) with 17 studies including both men and women. Sixteen studies were conducted in forensic mental health services and nine in non-forensic mental health services, across nine countries: UK (n = 8), Netherlands (n = 5), USA (n = 4), Canada (n = 2), Sweden (n = 2), Australia (n = 1), Norway (n = 1), Germany (n = 1), and Ireland (n = 1). Additional study characteristics are presented in Table 2. Figure 3 PRISMA flow diagram of study selection Table 2 Study characteristics Study Country Sample Characteristics Clinical Characteristics Method of Assessing Dynamic Risk Factors Aggressive Outcome Quality Assessment (0-9) Forensic Mental Health Services (n = 16) Abidin (2013) et al. Men = 94 (94%) Women = 6 (6%) Mean Age = 40.45 SD = 12.8 Range = 21.1 - 69.3 Psychosis = 85 (85%) Affective Disorder = 12 (12%) Intellectual Disability = 3 (3%) Structured Risk Assessment Physical aggression towards others and autoaggression, assessed through routine incident reporting forms, daily nurse management logs, and statutory forms for seclusion and restraint 6 Ireland Xxxxxxx (2016) et al. Netherlands Men = 69 (100%) Mean Age = 37.9 SD = 7.9 Affective Disorder = 5 (7.2%) Personality Disorder = 69 (100%) Substance-use Disorders = 53 (76.8%) Developmental Disorder = 15 (21.7%) Other = 6 (8.7%) No Diagnosis = 10 (14.5%) Emotional Stroop, Signal Detection Task, Graded Emotion Recognition Task Physical and verbal aggression towards others, and property aggression, assessed using the Modified Overt Aggression Scale 6 xx Xxxxx (2019) et al. Netherlands Men = 68 (68%) Women = 32 (32%) Mean Age = 32.01 SD = 9.02 Range = 18-57 Intellectual Disability = 100 (100%) Passive Remote Monitoring Device Physical and verbal aggression towards others, autoaggression, and property aggression, assessed using the Modified Overt Aggression Scale+ 8 Xxxxxxx & Xxxxxx (2004) UK Men = 44 (100%) Mean Age = 44 Range = 19-65 Psychosis = 24 (54.5%) Affective Disorder = 3 (6.8%) Personality Disorder = 11 (25%) Comorbid Psychosis/Personality Disorder = 6 (13.6%) Structured Risk Assessment Physical and verbal aggression towards others, and property aggression, assessed using hospital incident reporting forms 6 Xxxxx et al. (2015) USA Men = 109 (31%) Women = 239 (69%) Age Not Specified Not Applicable (Staff Members) Staff Survey Physical aggression towards others, assessed using an unvalidated Likert Scale 8 Lin...
Study Characteristics. Studies that met inclusion criteria and their individual characteristics, including location of study, and the population involved, are listed in Tables 1 and 2. For both groups (cancer care and cancer screening) of data, study subjects are defined as FtMs, MtFs, gender queer and gender non-confirming individuals, healthcare providers, and transgender health advocates. Fifteen studies were done in the United States (most, but not all, were conducted in large, urban cities) and one study was done in Canada. The 9 studies on cancer screening in transgender individuals are summarized in Table 1. Seven of these studies used qualitative methods. Of those, three used focus groups; one with transgender health advocates, and another two with medical providers. Four qualitative studies used in-person and phone interviews of transgender patients. Other studies used quantitative methods; three studies used online surveys that targeted transgender individuals and three used retrospective chart review of patient data (one of these studies also looked retrospectively at the subjective data directly taken from patient charts completed by providers). The majority, 6 out of 9, studies focused on cervical cancer screening. One looked at breast cancer screening, one looked at both breast and cervical cancer screening, and one remaining study looked at anal cancer screening. Seven studies published from 2008 through 2016 examined barriers to and facilitators of cancer care in transgender people (Table 2). Two of those studies used qualitative methods; both based on in-person interviews (one study was an interview with a single transgender patient). Five studies used quantitative methods; one study used interview data of transgender cancer patients from the Cancer’s Margins project, which studies the experiences of transgender people with cancer, in Canada, three studies used internet questionnaires, administered one to OB/GYN providers, oncology practitioners and cancer patients, and one study used retrospective review of survey data from the LIVESTRONG dataset (a national survey of cancer survivors in the United States, which included a subset of transgender patients).
Study Characteristics. 15 3.1.3 Measurement of Social rank and related constructs 16
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Study Characteristics. Study characteristics are reported in table 1. The majority of the studies employed a cross-sectional design (N= 12). Three studies utilised a prospective cohort study design (Brugnera et al., 2019; Xxxxxx, Xxxxx & Xxxxxxx, 2012; Xxxxxxx, Xxxxx & Xxxxxxx, 2010). Two studies did not report the length of time between baseline data collection and follow-up, but only described it as pre- and post-treatment (Xxxxxx, Xxxxx & Xxxxxxx, 2012; Xxxxxxx, Xxxxx & Xxxxxxx, 2010). In the other study (Brugnera et al., 2019), the length of time between baseline data collection and follow-up was 12 months. One study (Xx & Xxxxx, 2020) employed an ecological momentary assessment (EMA), which assessed participants repeatedly in their natural environment in real time. The majority of studies included a control group of healthy participants (i.e. not having a diagnosis of ED) (N= 11).

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  • Study Population ‌ Infants who underwent creation of an enterostomy receiving postoperative care and awaiting enterostomy closure: to be assessed for eligibility: n = 201 to be assigned to the study: n = 106 to be analysed: n = 106 Duration of intervention per patient of the intervention group: 6 weeks between enterostomy creation and enterostomy closure Follow-up per patient: 3 months, 6 months and 12 months post enterostomy closure, following enterostomy closure (12-month follow-up only applicable for patients that are recruited early enough to complete this follow-up within the 48 month of overall study duration).

  • PURPOSE AND IMPLEMENTATION This Umbrella Agreement (hereinafter referred to as the "Agreement" or "Umbrella Agreement") shall be for the purpose of collaborative research, development, and testing opportunities on various topics of mutual interest to enable advanced understanding of aeronautics, science, and space systems research and development and to provide workforce development in Science, Technology, Engineering, and Mathematics (STEM) while furthering NASA’s research and development goals. The Parties shall execute one (1) Annex Agreement (hereinafter referred to as the "Annex") concurrently with this Umbrella Agreement. The Parties may execute subsequent Annexes under this Umbrella Agreement consistent with the purpose and terms of this Umbrella Agreement. This Umbrella Agreement shall govern all Annexes executed hereunder; no Annex shall amend this Umbrella Agreement. Each Annex will detail the specific purpose of the proposed activity, responsibilities, schedule and milestones, and any personnel, property, or facilities to be utilized under the task. This Umbrella Agreement takes precedence over any Annexes. In the event of a conflict between the Umbrella Agreement and any Annex concerning the meaning of its provisions, and the rights, obligations and remedies of the Parties, the Umbrella Agreement is controlling.

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  • Study An application for leave of absence for professional study must be supported by a written statement indicating what study or research is to be undertaken, or, if applicable, what subjects are to be studied and at what institutions.

  • Screening After you sign and date the consent document, you will begin screening. The purpose of the screening is to find out if you meet all of the requirements to take part in the study. Procedures that will be completed during the study (including screening) are described below. If you do not meet the requirements, you will not be able to take part in the study. The study investigator or study staff will explain why. As part of screening, you must complete all of the items listed below: • Give your race, age, gender, and ethnicity • Give your medical history o You must review and confirm the information in your medical history questionnaire • Give your drug, alcohol, and tobacco use history • Give your past and current medication and treatment history. This includes any over-the-counter or prescription drugs, such as vitamins, dietary supplements, or herbal supplements, taken in the past 28 days • Height and weight will be measured • Physical exam will be done • Electrocardiogram (ECG) will be collected. An ECG measures the electrical activity of the heart • You may be tested for COVID-19 o Blood tests for human immunodeficiency virus (HIV), hepatitis B, and hepatitis C o Blood tests to see how your blood clots ▪ Fibrinogen ▪ PT/INR/aPTT o Blood tests for amylase and lipase (enzymes that help with digestion, Part B only) o Blood tests for a lipid (fats) panel (Part B only) ▪ Total cholesterol ▪ Triglycerides ▪ HDL ▪ Direct HDL o Blood tests to check your thyroid function (Part B and Part C only) ▪ TSH ▪ Free T4 o Urine to test for drugs of abuse (illegal and prescription) o Urine tests to check your albumin/ creatinine ratio o Females who have not had a period for at least 12 months in a row will have a blood hormone test to confirm they cannot have children • The study investigator may decide to do an alcohol breath test • The use of proper birth control will be reviewed (males only) • You will be asked “How do you feel?” HIV, hepatitis B, and hepatitis C will be tested at screening. If anyone is exposed to your blood during the study, you will have these tests done again. If you have a positive test, you cannot be in or remain in the study. HIV is the virus that causes acquired immunodeficiency syndrome (AIDS). If your HIV test is positive, you will be told about the results. It may take weeks or months after being infected with HIV for the test to be positive. The HIV test is not always right. Having certain infections or positive test results may have to be reported to the State Department of Health. This includes results for HIV, hepatitis, and other infections. If you have any questions about what information is required to be reported, please ask the study investigator or study staff. Although this testing is meant to be private, complete privacy cannot be guaranteed. For example, it is possible for a court of law to get health or study records without your permission.

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  • Protocol The attached Protocol shall be an integral part of this Agreement.

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  • Review Protocol A narrative description of how the Claims Review was conducted and what was evaluated.

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