Camela S. McDougald
Duke University
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Publication
Featured researches published by Camela S. McDougald.
Journal of The National Medical Association | 2009
Christopher L. Edwards; Marquisha Green; Chante Wellington; Malik Muhammad; Mary Wood; Miriam Feliu; Lekisha Edwards; LaBarron K. Hill; John J. Sollers; Crystal Barksdale; Elwood Robinson; Camela S. McDougald; Mary Abrams; Keith E. Whitfield; Goldie S. Byrd; Bob Hubbard; Monique G. Cola; Laura DeCastro; Janice McNeil
There is a strong relationship between suicidal ideation, suicide attempts, and depression. Rates of successful suicides are relatively high among the chronically ill compared to other populations but are reduced with treatment. Depression and suicide rates also often differ among blacks as compared to other populations. Using survey methods, we evaluated self-reported rates of depression, suicidal ideation, and suicide attempts in 30 male and 37 female black patients with sickle cell disease (SCD). SCD is a condition characterized by chronic, unpredictable pains and psychosocial distress. Thirty-six percent of the sample self-reported depression in the past 30 days, while 22 percent of the sample exhibited scores on the Beck Depression Inventory indicative of mild or greater depression (mean BDI, 8.31 +/- 7.79). Twenty-nine percent of patients indicated an episode of suicidal ideation and 8%, a suicidal attempt in their lifetime. Thirty-three percent reported treatment by a mental health professional. We conclude that there is a continuing need for mental health services in the management of depressed affect and risk for suicide among patients with SCD. Standards of clinical care must remain flexible to accommodate the mental health needs of this population of patients.
The Clinical Journal of Pain | 2007
Jennifer J. Pells; Christopher L. Edwards; Camela S. McDougald; Mary Wood; Crystal Barksdale; Jude Jonassaint; Brittani Leach-Beale; Goldie S. Byrd; Markece Mathis; Myleme O. Harrison; Miriam Feliu; Lekisha Edwards; Keith E. Whitfield; Lesco Rogers
ObjectivesFear of movement (ie, kinesiophobia) has emerged as a significant predictor of pain-related outcomes including disability and psychologic distress across various types of pain (eg, back pain, headache, fibromyalgia, complex regional pain syndrome). However, no research has examined the prevalence of kinesiophobia in adults with sickle cell disease (SCD). The purpose of this study was to assess the degree of kinesiophobia reported by African American men and women with SCD and to determine whether kinesiophobia is related to pain and psychologic distress in this population. MethodsSixty-seven men and women with SCD recruited from a comprehensive sickle cell treatment program in a large academic medical center completed questionnaires that assess fear of movement, pain and pain interference, and psychologic distress. ResultsParticipants reported levels of kinesiophobia (M=30.48, SD=7.55) that were comparable to those obtained for patients with low back pain and fibromyalgia. Although pain levels did not differ by sex, men reported greater kinesiophobia than women (P=0.02). As hypothesized, higher levels of kinesiophobia were associated with greater psychologic distress, particularly Phobic Anxiety (r=0.35), Psychoticism (r=0.29), Somatization (r=0.45), Anxiety (r=0.35), Obsessive-compulsive (r=0.34), Interpersonal Sensitivity (r=0.25), Depression (r=0.29), and all 3 summary indices of the SCL-90-R (all Ps<0.05). DiscussionAlthough and historically, pain associated with SCD has not been considered in the context of fear of movement, findings suggest that both kinesiophobia and sex are relevant constructs for consideration in understanding pain-related outcomes in SCD. Though our results require replication, this study suggests that greater kinesiophobia is associated with greater pain and psychologic distress.
Neuropsychiatric Disease and Treatment | 2008
Christopher L. Edwards; Renee Raynor; Miriam Feliu; Camela S. McDougald; Stephanie Johnson; Donald E. Schmechel; Mary Wood; Gary G. Bennett; Patrick Saurona; Melanie J. Bonner; Laura DeCastro; Mary Abrams; Patrick E. Logue; Lekisha Edwards; Salutario Martinez
Traditionally, neuropsychological deficits due to Sickle Cell Disease (SCD) have been understudied in adults. We have begun to suspect, however, that symptomatic and asymptomatic Cerebrovascular Events (CVE) may account for an alarming number of deficits in this population. In the current brief review, we critically evaluated the pediatric and adult literatures on the neurocognitive effects of SCD. We highlighted the studies that have been published on this topic and posit that early detection of CVE via neurocognitive testing, neuropsychiatric evaluations, and neuroimaging may significantly reduce adult cognitive and functional morbidities.
Journal of The National Medical Association | 2008
Christopher L. Edwards; Gary G. Bennett; ScD Kathleen Y. Wolin; Stephanie Johnson; Sherrye Fowler; Keith E. Whitfield; Sandy Askew; Dorene MacKinnon; Camela S. McDougald; Robert Hubbard; Chante Wellington; PsyD Miriam Feliu; Elwood Robinson
Blacks experience disproportionately elevated rates of tobacco-related morbidity and mortality. Blacks experience delayed smoking initiation relative to other racial/ethnic groups, highlighting the importance of examining smoking correlates occurring in late adolescence/early adulthood. The current study reports data collected as part of an ongoing collaborative effort to assess alcohol and drug use on the campuses of historically black colleges and universities (HBCUs). Two-thousand, two-hundred, seventy-seven African-American subjects, aged 20.3 +/- 3.9 (range 18-53), completed the CORE Alcohol and Drug survey and a brief demographic questionnaire. Results indicated that 90% of all subjects overestimated the rate of smoking among their peers. Overestimating was associated with a > 80% increase in the risk of smoking. These data highlight the need to correct misinformation regarding smoking norms among students at some HBCUs.
Aging & Mental Health | 2008
Keith E. Whitfield; Christopher L. Edwards; Dwayne T. Brandon; Camela S. McDougald
Depression is typically considered relative to individuals and thought to originate from both biological and environmental factors. However, the environmental constraints and insults that African Americans experience likely influence the concordance by age and gender for depression scores among adult African American twins. Monozygotic (MZ) (n = 102) and Dizygotic (DZ) (n = 110) twins, age 25–88 years in the Carolina African American Twin Study of Aging were examined using an 11-item version of the CES-D measure of depressive symptomatology. Those participants with scores above nine were considered depressed. Overall, the MZ pairs had a higher concordance than the DZ pairs implying genetic influence. Both MZ and DZ males had higher concordances than either female zygosity groups. The difference between the concordance rates for MZ and DZ twin pairs was greater in males than females. By age group, the difference between the concordance rates for younger MZ and DZ twin pairs was much larger than for older pairs. The results suggest that, even though African Americans may be at risk for depression due to contextual/environmental factors, genetic influences remain important.
Journal of The National Medical Association | 2010
Chante Wellington; Christopher L. Edwards; Janice McNeil; Mary Wood; Benjamin Crisp; Miriam Feliu; Goldie S. Byrd; Camela S. McDougald; Lekisha Edwards; Keith E. Whitfield
The unpredictable nature of sickle cell disease (SCD) and its social and environmental consequences can produce an unhealthy and almost exclusive focus on physical functioning. At the upper range of this focus on health concerns is somatization. In the current study, using 156 adult patients (55.13% female, 86) with SCD, mean age 35.59 +/- 12.73, we explored the relationship of somatization to pain. We found somatization to be predictive of pain severity and current pain intensity as well as a range of averaged indices of pain over time (p < .0001). We further found somatization to be predictive of a range of negative psychological experiences to include depression, anxiety, and hostility (p < .0001). We interpret these data to suggest that patients with SCD who have a propensity to focus exclusively on their health or are more sensitive to minor changes in their health status (somatization) may also be more likely to report greater concerns about their health and higher ratings of pain.
Revue canadienne de recherche en sciences infirmières | 2012
Janice Collins-McNeil; Christopher L. Edwards; Bryan C. Batch; Debra Benbow; Camela S. McDougald; Daphne Sharpe
Journal of African American Studies | 2009
Cara O’Connell-Edwards; Christopher L. Edwards; Amy B. Wachholtz; Mary Wood; Malik Muhammad; Brittani Leach-Beale; Rebecca A. Shelby; Camela S. McDougald; M. Ojinga Harrison; Miriam Feliu; Lekisha Edwards; Keith E. Whitfield; Marcellus M. Merritt; Chante Wellington; Goldie S. Byrd; Janice McNeil; Henry L. Edmonds; Elwood Robinson
Journal of African American Studies | 2009
Camela S. McDougald; Christopher L. Edwards; Mary Wood; Chante Wellington; Miriam Feliu; Keisha O’Garo; Lekisha Edwards; Elwood Robinson; Keith E. Whitfield; Sherry C. Eaton; Kai Morgan; Goldie S. Byrd; John J. Sollers; Monique G. Cola; Cara F. O’Connell
Journal of The National Medical Association | 2006
Christopher L. Edwards; Annelle Primm; Stephanie Johnson; Miriam Feliu; Keisha O'Garo; Gary G. Bennett; Elwood Robinson; Camela S. McDougald; Goldie S. Byrd; Ojinga Harrison; Keith E. Whitfield; Alvin Killough
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North Carolina Agricultural and Technical State University
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