This community-based intervention is an encouraging option for behavioral treatment of UI. Public health models may be particularly appropriate with moderate levels of urinary incontinence.

Black and Hispanic populations perceive their skin cancer risk to be low and are less likely to use sun protection strategies. We conducted formative research to understand knowledge, awareness, beliefs, and behaviors among these groups. In 2017, eighteen focus groups were conducted with black and Hispanic respondents(18–44 years) in four US cities. Groups were segmented by participant characteristics associated with elevated or lower risk for skin cancer, by race/ethnicity, gender, and age. A professional moderator followed a semi-structured discussion guide, and focus group transcripts were analyzed using conventional content analysis and NVIVO 11 Software. Most participants perceived themselves to be at low skin cancer risk due to their “darker skin tone” and/or “lack of family history.” Skin cancer signs and symptoms were more inconsistently reported by blacks than Hispanics. Few participants reported regular sun protection behaviors. Those who did used sunscreen, wore protective clothing, and had elevated risk based on sun sensitivity or UV exposure. While most participants recalled family discussions (as youth) about sunscreen and sun protection, the understood intent was to warn against “further skin darkening” or to “prevent aging,” not to reduce sun burns or skin cancer risk. Tanning bed use was low across all segments, especially among black respondents. Tailored skin cancer prevention campaigns need to address misperceptions about risks and benefits of skin cancer prevention behaviors among black and Hispanic populations. Families, peer groups, and healthcare providers need to be engaged in the creation of educational interventions and messaging efforts that target these populations.

The intervention affected condition-specific quality of life and self-management but not general HRQL. The intervention's impact on quality of life involves change in how the condition is seen as impacting on life and on selection of self-management behaviors.

This article documents a collaborative health agency-university community demonstration project on urinary incontinence in older women. The basic program-research division of respon sibility was blurred substantially in this collaboration. The article focuses on a telephone survey of 321 elderly women conducted as part of a needs assessment, which also served as baseline data in the evaluation of a public education initiative. The survey provided information for defin ing target populations, shaping educational messages, and selecting communication channels. The prevalence of involuntary urine loss was 34%, with 20% of all women reporting weekly in continence. There were few differences by continence status in health, sociodemographic char acteristics, orbeliefs about incontinence. Women used many communication channels for health information and had a preference for information from health professionals. Factors that con tributed to the collaborative relationship included technical expertise, diversity of expertise and perspectives, and the enhancement of capacity in collaborators.

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