Temporal Integration of Information in Orthographic Priming

We present a theoretical framework for studying the integration of information over time in experimental paradigms involving the successive presentation of printed strings of letters with varying orthographic overlap (orthographic priming). This framework is expressed as a set of six processing principles, five of which are derived directly from the interactive activation model of orthographic processing (McClelland & Rumelhart, 1981), and an additional sixth principle relative to a hypothesized inhibitory resetmechanism. The validity of these principles are evaluated with respect to data obtained from different variants of the orthographic priming paradigm, and related paradigms.     

Finding Voice: The Photovoice Method of Data Collection in HIV and AIDS-Related Research

This study examined the efficacy of photovoice as a research technique to explore the lives of children and families living in the context of HIV and AIDS. Participants were volunteers at a Day Care and Support Centre (n=18), and members of a community support group consisting of People Living with AIDS (n=5). The findings revealed that the photovoice method is particularly useful for dealing with the ‘unspoken’ lived experience of children and families.     

Communicating BRCA1/2 genetic test results within the family: A qualitative analysis

Genetic testing for BRCA1/2 mutations associated with hereditary breast and ovarian cancer reveals significant risk information about one's chances of developing cancer. It is important to study communication processes in families where members are undergoing genetic testing because the information received is crucial not just to the individual concerned but also to other members of the biological family. This study investigates family communication of BRCA1/2 test results from both the informants’ and recipients’ perspectives. A total of 10 female patients and 22 of their relatives were interviewed. Patients’ and their relatives described feelings of responsibility for sharing genetic information within the family to enable others to reduce their risks of developing cancer. However, there were limits to an individuals’ responsibility once key family members had been informed, who then had to take responsibility for continuing dissemination of information. Whilst there was an implicit responsibility to inform the family of a mutation, information was edited or withheld in the best interest of relatives, dependent upon their perceived emotional readiness, resilience and current life stage and circumstances. The pre-existing family culture and the impact previous cancer diagnoses had upon the family also influenced the process of communication. Findings are discussed in relation to extant literature and implications for clinical practice are considered.     

Unintended Consequences of EEO Enforcement Policies: Being Big is Worse than Being Bad

In enforcing the Civil Rights Acts of 1964 and 1991, it is often critical to determine whether a challenged procedure has systematic adverse impact. The use of statistical significance tests to make this determination has the perverse consequence that the size of an organization or an applicant pool has more impact on determining adverse impact than the extent to which procedures actually discriminate. That is, it is worse to be big than to be bad. We use Monte Carlo studies to illustrate this unforeseen consequence of current enforcement policies and note that a broader definition of adverse impact is clearly warranted.     

Book review

Individualizing clinical assessments of the life‐world

Fischer, Constance T. Individualizing Psychological Assessment. Monterey, CA: Brooks/Cole, 1985, 410 pp.

The body in psychotherapy

Smith, W. L. Edward. The Body In Psychotherapy. Jefferson, NC: McFarland & Company, Inc., 1985, 189 pp., $18.95.     

Religious belief,age, and sexual orientation on attributions of younger and older gay and heterosexual men

Using 4 vignettes and 20 response items, this exploratory study investigated attributions about older or younger gay or heterosexual men with a history of multiple sex partners, substance abuse, and legal problems. The character is diagnosed with a terminal illness and two options for care: no treatment or an aggressive treatment protocol with a small chance of recovery. When controlling for respondents’ (N?=?324) religious identification, frequency of attendance at religious services, and ethno-cultural identification, a General Linear Model was significant (F?=?57.014, df?=?20, p?<?.001). Differences in the vignette responses centred on perceptions of quality of life, the character's lifestyle, and suicide.     

Circumstance of Birth: Life on the Color Line

The article describes how my privileged social-location in a White, middle-class suburb shaped my interest in unpacking White privilege and White blindness. I define and elaborate on the implications of one’s “social location.” In unpacking the influences from, and implications of, my social location, I describe the development of a clinical attitude that aims at inclusive dialogue, with special emphasis on humility, dignity, and emotional courage.