36 research outputs found

    Training Programs for Improving Communication about Medical Research and Clinical Trials: A Systematic Review

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    Objectives: The aim of this article is to provide recommendations on the structure, materials, and outcomes that should be adopted for communication training programs designed to improve clinical trial education for patients

    Prevalence and Correlates of Invitation to Participate in Clinical Trials among US Adults

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    Clinical trials are essential to modern medicine, but several barriers, including poor communication, hamper their successful completion. We examined the prevalence and correlates of invitation to participate in clinical trials among a nationally-representative sample of US adults using survey responses from the 2020 HINTS (Cycle 5). Analyses were conducted in 2021. Overall, 9% of respondents reported being invited to a clinical trial, a prevalence that is nearly half of previously reported rates in convenience samples recruited from health care settings. Compared to non-Hispanic Whites, Black respondents reported the higher prevalence of invitation (16.0%) whereas Asian respondents reported the lowest (2%). Prevalence of clinical trial invitation was significantly higher for the 65–74 age and the 75 + age groups. Prevalence of invitation was significantly higher among college graduates (12.0%) and lower for those residing in rural areas/small towns compared to metropolitan areas. Invitation was significantly higher among cancer patients/survivors (16.0%), patients with diabetes (11.7%) and with chronic lung disease (16.7%). Provider and patient factors there were associated with higher invitation rates included using web devices to communicate with providers or to aid health-related discussions, having a specific medical provider, and looking for health information online. This study establishes a population-based prevalence of clinical trial communication that can be monitored as health care providers/organizations increase their focus on enrollment activities. Targeted interventions to improve communication about clinical trials are needed to address socio-demographic disparities and are particularly important for Asian patients, patients with lower income, and those living in rural areas

    Mobile phone messaging to promote uptake of HIV testing among migrant African communities in the UK

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    Background: In the UK, African communities are a focus of public health efforts to increase uptake of HIV testing. Mobile phone interventions may be an innovative way of reaching migrant groups who are known to face multiple obstacles in accessing mainstream health services. This paper presents findings from a feasibility study that used participatory approaches to investigate the use of a text messaging intervention to encourage HIV testing among migrant African communities. Methods: Participants were recruited in the city of Nottingham by a team of community researchers. They were sent two text messages per week (one on HIV and one on general health) for 12 weeks. Baseline and follow-up questionnaires were completed to measure HIV testing behaviour, HIV related knowledge and attitudes and general health. Participants’views on the intervention were solicited. Results: One hundred and sixty-nine participants were enrolled in the study. Follow up data on HIV testing was obtained for 76 participants (45%) and complete follow up measures were available from 60 participants (36%). Eight reported seeking an HIV test during the study period. There were statistically significant positive changes in attitudes about HIV, and a trend towards increased knowledge about HIV. One third of participants reported improvements in physical activity levels, diet, and stress management following the intervention. The intervention messages and structure were positively evaluated. Conclusions: Well-designed mobile phone messaging proved to be a feasible and acceptable intervention to promote both HIV testing and lifestyle behaviours among African migrant communities in the UK. When co-constructed with communities, they hold considerable promise for overcoming some of the health-related barriers faced by migrant populations in new countries. Future research and service development should focus on exploiting and evaluating this potential in relation to other key health priorities

    Assessing Communication Practice during Clinical Trial Recruitment and Consent: The Clinical Trial Communication Inventory (CTCI)

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    The development and evaluation of training programs with the potential to improve informed consent and accrual to clinical trials depend heavily on the ability to measure outcomes of these trainings. In this chapter, we present the development of an instrument, the clinical trial communication inventory (CTCI). Data were collected from 87 clinical research professionals at three academic medical centers, which were analyzed using factor analytic methods and reliability testing procedures. This testing resulted in eight subscales representing verbal, nonverbal, and privacy protection behaviors. While the final CTCI instrument would benefit from further validity testing, it represents a resource that can be used to evaluate future trainings of research professionals

    Occa, Aurora

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    Formative Research to Create Culturally Sensitive HPV Vaccine Messages for Middle-School Children

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    HPVs (Human Papilloma Viruses) are the cause of several diseases and types of cancer, but infections can be prevented through a vaccine that children are recommended to receive when they are about 12 years of age. Communicating with children about HPV is an important albeit underdeveloped task. This is especially critical in countries such as Italy, were the HPV vaccination rate is dropping. To understand Italian middle-school children’s communication challenges, needs and preferences, and to provide evidence to inform the development of targeted and culturally-sensitive messages about HPV for them, this study adopted a multi-method participatory approach consisting of focus group discussions and participatory drawings. Results indicated that children (N = 54) wanted to be actively engaged in decisions about their health but faced several communication challenges, including adults’ language and attitude. Children struggled to retrieve reliable information on their own. They provided specific information on the sources and the strategies they would want adults to adopt. Results helped to identify positive and negative behaviours among these themes, as well as key resources to be leveraged in the development of HPV-related messages. The communication strategies identified in this study may help parents, healthcare providers, and caregivers to improve their communication with children
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