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Dive into the research topics where Colleen M. McBride is active.

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Featured researches published by Colleen M. McBride.


Annual Review of Public Health | 2010

The Behavioral Response to Personalized Genetic Information: Will Genetic Risk Profiles Motivate Individuals and Families to Choose More Healthful Behaviors?

Colleen M. McBride; Laura M. Koehly; Saskia C. Sanderson; Kimberly A. Kaphingst

This report describes the use of information emerging from genetic discovery to motivate risk-reducing health behaviors. Most research to date has evaluated the effects of information related to rare genetic variants on screening behaviors, in which genetic risk feedback has been associated consistently with improved screening adherence. The limited research with common genetic variants suggests that genetic information, when based on single-gene variants with low-risk probabilities, has little impact on behavior. The effect on behavioral outcomes of more realistic testing scenarios in which genetic risk is based on numerous genetic variants is largely unexplored. Little attention has been directed to matching genetic information to the literacy levels of target audiences. Another promising area for research is consideration of using genetic information to identify risk shared within kinship networks and to expand the influence of behavior change beyond the individual.


Addictive Behaviors | 1997

Reasons for quitting: Intrinsic and extrinsic motivation for smoking cessation in a population-based sample of smokers

Susan J. Curry; Louis C. Grothaus; Colleen M. McBride

An intrinsic-extrinsic model of motivation for smoking cessation is extended to a population-based sample of smokers (N = 1,137), using a previously validated Reasons for Quitting (RFQ) scale. Psychometric evaluation of the RFQ replicated the model that includes health concerns and self-control as intrinsic motivation dimensions and immediate reinforcement and social influence as extrinsic motivation dimensions. Compared to volunteers, the population-based sample of smokers reported equivalent health concerns, lower self-control, and higher social influence motivation for cessation. Within the population-based sample, women compared to men were less motivated to quit by health concerns and more motivated by immediate reinforcement; smokers above age 55 expressed lower health concerns and higher self-control motivation than smokers below age 55. Higher baseline levels of intrinsic relative to extrinsic motivation were associated with more advanced stages of readiness to quit smoking and successful smoking cessation at a 12-month follow-up. Among continuing smokers, improvement in stage of readiness to quit over time was associated with significant increases in health concerns and self-control motivation.


American Journal of Public Health | 1999

Prevention of relapse in women who quit smoking during pregnancy.

Colleen M. McBride; Susan J. Curry; Harry A. Lando; Phyllis L. Pirie; Lou Grothaus; Jennifer C. Nelson

OBJECTIVES This study is an evaluation of relapse prevention interventions for smokers who quit during pregnancy. METHODS Pregnant smokers at 2 managed care organizations were randomized to receive a self-help booklet only, prepartum relapse prevention, or prepartum and postpartum relapse prevention. Follow-up surveys were conducted at 28 weeks of pregnancy and at 8 weeks, 6 months, and 12 months postpartum. RESULTS The pre/post intervention delayed but did not prevent postpartum relapse to smoking. Prevalent abstinence was significantly greater for the pre/post intervention group than for the other groups at 8 weeks (booklet group, 30%; prepartum group, 35%; pre/post group, 39%; P = .02 [different superscripts denote differences at P < .05]) and at 6 months (booklet group, 26%, prepartum group, 24%; pre/post group, 33%; P = .04) postpartum. A nonsignificant reduction in relapse among the pre/post group contributed to differences in prevalent abstinence. There was no difference between the groups in prevalent abstinence at 12 months postpartum. CONCLUSIONS Relapse prevention interventions may need to be increased in duration and potency to prevent post-partum relapse.


Genetics in Medicine | 2009

The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop

Muin J. Khoury; Colleen M. McBride; Sheri D. Schully; John P. A. Ioannidis; W. Gregory Feero; A. Cecile J. W. Janssens; Marta Gwinn; Denise G. Simons-Morton; Jay M. Bernhardt; Michele Cargill; Stephen J. Chanock; George M. Church; Ralph J. Coates; Francis S. Collins; Robert T. Croyle; Barry R. Davis; Gregory J. Downing; Amy Duross; Susan Friedman; Mitchell H. Gail; Geoffrey S. Ginsburg; Robert C. Green; Mark H. Greene; Philip Greenland; Jeffrey R. Gulcher; Andro Hsu; Kathy Hudson; Sharon L.R. Kardia; Paul L. Kimmel; Michael S. Lauer

The increasing availability of personal genomic tests has led to discussions about the validity and utility of such tests and the balance of benefits and harms. A multidisciplinary workshop was convened by the National Institutes of Health and the Centers for Disease Control and Prevention to review the scientific foundation for using personal genomics in risk assessment and disease prevention and to develop recommendations for targeted research. The clinical validity and utility of personal genomics is a moving target with rapidly developing discoveries but little translation research to close the gap between discoveries and health impact. Workshop participants made recommendations in five domains: (1) developing and applying scientific standards for assessing personal genomic tests; (2) developing and applying a multidisciplinary research agenda, including observational studies and clinical trials to fill knowledge gaps in clinical validity and utility; (3) enhancing credible knowledge synthesis and information dissemination to clinicians and consumers; (4) linking scientific findings to evidence-based recommendations for use of personal genomics; and (5) assessing how the concept of personal utility can affect health benefits, costs, and risks by developing appropriate metrics for evaluation. To fulfill the promise of personal genomics, a rigorous multidisciplinary research agenda is needed.


Psychosomatic Medicine | 2001

Depressive symptoms, menopausal status, and climacteric symptoms in women at midlife.

Hayden B. Bosworth; Lori A. Bastian; Maggie Kuchibhatla; David C. Steffens; Colleen M. McBride; Celette Sugg Skinner; Barbara K. Rimer; Ilene C. Siegler

Objective Previous studies have found increased rates of depression in women aged 45 to 54 years, but the factors that influence these rates are not understood. It was assessed whether higher rates of depressive symptoms were associated with menopausal status, climacteric symptoms, and use of hormone replacement therapy. Design Cross-sectional survey. Setting Community sample. Methods Data are from 581 women ages 45 to 54 years who were interviewed by telephone between October 1998 and February 1999. Measures Depression was measured with the abbreviated CES-D, a depressive symptoms screening measure. Women’s reported perception of menopausal stage, frequency of periods in the preceding 12 months, and history of oophorectomy were used to classify their menopausal status into four categories: (1) no indication of menopause; (2) close to menopause; (3) had begun menopause; and (4) had completed menopause. Results There were 168 women (28.9%) who reported a high level (≥10) of depressive symptoms when the abbreviated CES-D was used. In a logistic-regression analysis, significant factors associated with increased depressive symptoms included physical inactivity, inadequate income, use of estrogen/progesterone combination, and presence of climacteric symptoms (trouble sleeping, mood swings, or memory problems). Menopausal status was not associated with depressive symptoms. Conclusions In this sample of women age 45 to 54 years, climacteric symptoms but not menopausal status were associated with higher rates of depressive symptoms.


American Journal of Public Health | 1998

Differences in preconceptional and prenatal behaviors in women with intended and unintended pregnancies.

Wendy L. Hellerstedt; Phyllis L. Pirie; Harry A. Lando; Susan J. Curry; Colleen M. McBride; Louis C. Grothaus; Jennifer C. Nelson

OBJECTIVES This study examined whether pregnancy intention was associated with cigarette smoking, alcohol drinking, use of vitamins, and consumption of caffeinated drinks prior to pregnancy and in early pregnancy. METHODS Data from a telephone survey of 7174 pregnant women were analyzed. RESULTS In comparison with women whose pregnancies were intended, women with unintended pregnancies were more likely to report cigarette smoking and less likely to report daily vitamin use. Women with unintended pregnancies were also less likely to decrease consumption of caffeinated beverages or increase daily vitamin use. CONCLUSIONS Pregnancy intention was associated with health behaviors, prior to pregnancy and in early pregnancy, that may influence pregnancy course and birth outcomes.


American Journal of Public Health | 1992

Smoking cessation in women concerned about weight.

Phyllis L. Pirie; Colleen M. McBride; Wendy L. Hellerstedt; Robert W. Jeffery; D Hatsukami; S Allen; Harry A. Lando

BACKGROUND Weight gain after smoking cessation is often cited by women smokers as a primary reason for not attempting to quit smoking or for relapsing after a cessation attempt. METHODS A randomized trial of 417 women smokers was conducted to test the addition of two weight control strategies to a smoking cessation program. Participants received the standard smoking cessation program, the program plus nicotine gum, the program plus behavioral weight control, or the program plus both nicotine gum and behavioral weight control. Weight and smoking status were measured at the end of treatment and at 6 and 12 months posttreatment. RESULTS Smoking cessation rates were highest in the group receiving the smoking cessation program plus nicotine gum. Weight gain did not vary by treatment condition, so its effect on relapse could not be examined by group. There was no significant relationship between weight gained and relapse in individuals. CONCLUSIONS The added behavioral weight control program was attractive to the participants and did not reduce smoking cessation rates. However, it did not produce the expected effect on weight, thereby restricting our ability to examine the effect of weight control on smoking cessation and relapse.


Psycho-oncology | 2000

Psychological impact of diagnosis and risk reduction among cancer survivors

Colleen M. McBride; Elizabeth C. Clipp; Bercedis L. Peterson; Isaac M. Lipkus; Wendy Demark-Wahnefried

Life‐threatening health events prompt psychological distress that may motivate individuals to reduce health risks. If so, interventions timed to take advantage of these ‘teachable moments’ could be particularly effective. To explore this association, early stage prostate and breast cancer patients were identified from a hospital‐based tumor registry within 6 years of diagnosis. These patients (n=920) completed a mailed survey assessing the Horowitz impact of events scale, risk behaviors and readiness to change the behaviors. Breast cancer patients, younger patients and those reporting poor health status reported the greatest impact of the cancer diagnosis. Impact was inversely associated with time from diagnosis for prostate, but not breast cancer patients. Prostate patients who reported exercising regularly had lower impact scores than those who were not exercising (medians: 0.13 vs 0.56, respectively; p=0.02). Breast patients who were eating five or more fruits and vegetables reported lower impact scores than those who were not eating the recommended servings (0.75 vs 1.06, respectively; p=0.03). Breast patients who were non‐smokers reported lower impact scores than smokers (0.88 vs 1.31, respectively; p=0.02). Prospective studies are needed to understand the psychological impact of cancer diagnosis and how it might facilitate or impede the adoption of health promoting behaviors. Copyright


Pain | 2008

Self-efficacy for managing pain, symptoms, and function in patients with lung cancer and their informal caregivers: associations with symptoms and distress.

Laura S. Porter; Francis J. Keefe; Jennifer Garst; Colleen M. McBride; Donald H. Baucom

&NA; This study examined self‐efficacy for managing pain, symptoms, and function in patients with lung cancer and their caregivers, and associations between self‐efficacy and patient and caregiver adjustment. One hundred and fifty‐two patients with early stage lung cancer completed measures of self‐efficacy, pain, fatigue, quality of life, depression, and anxiety. Their caregivers completed a measure assessing their self‐efficacy for helping the patient manage symptoms and measures of psychological distress and caregiver strain. Analyses indicated that, overall, patients and caregivers were relatively low in self‐efficacy for managing pain, symptoms, and function, and that there were significant associations between self‐efficacy and adjustment. Patients low in self‐efficacy reported significantly higher levels of pain, fatigue, lung cancer symptoms, depression, and anxiety, and significantly worse physical and functional well being, as did patients whose caregivers were low in self‐efficacy. When patients and caregivers both had low self‐efficacy, patients reported higher levels of anxiety and poorer quality of life than when both were high in self‐efficacy. There were also significant associations between patient and caregiver self‐efficacy and caregiver adjustment, with lower levels of self‐efficacy associated with higher levels of caregiver strain and psychological distress. These preliminary findings raise the possibility that patient and caregiver self‐efficacy for managing pain, symptoms, and function may be important factors affecting adjustment, and that interventions targeted at increasing self‐efficacy may be useful in this population.


American Journal of Preventive Medicine | 2009

Active Mothers Postpartum A Randomized Controlled Weight-Loss Intervention Trial

Truls Østbye; Katrina M. Krause; Cheryl A. Lovelady; Miriam C. Morey; Lori A. Bastian; Bercedis L. Peterson; Geeta K. Swamy; Rebecca J. Namenek Brouwer; Colleen M. McBride

BACKGROUND Pregnancy may contribute to overweight and obesity. PURPOSE The primary objective of Active Mothers Postpartum was to promote a reduction in BMI through 24-months postpartum via sustainable lifestyle changes. DESIGN Behavioral intervention RCT to enhance postpartum weight loss. SETTING/PARTICIPANTS A total of 450 overweight or obese women, enrolled 6-weeks postpartum, were recruited through obstetrics clinics and community posters in the Durham NC area. INTERVENTION Intervention participants were offered eight healthy-eating classes, ten physical-activity classes, and six telephone-counseling sessions over 9 months. MAIN OUTCOME MEASURES Changes from baseline (6-weeks postpartum) to 1-month post-intervention (12-months postpartum) in: (1) diet (caloric intake, calories from fat, intake of certain foods); (2) physical activity (self-reported physical activity, television time); and (3) weight (collected 2004-2007, analyzed 2007-2008). RESULTS Mean weight loss was 0.90 kg (+/-5.1 kg) in the intervention group and 0.36 kg (+/-4.9 kg) in the control group; this difference was not significant. There were also no significant group differences in improvement of diet or increased physical activity. In secondary analyses, there was a positive bivariate relationship between classes attended and weight loss (p=0.01). CONCLUSIONS There were no significant differences among the arms in diet, physical activity, or weight change. Home-based interventions via mail, telephone, or Internet/e-mail may be more feasible and successful in this population. The postpartum period is an important phase in womens lives with regard to weight retention, but engaging them during this busy period remains a challenge. TRIAL REGISTRATION NCT00212251.

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Susan J. Curry

Group Health Cooperative

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Laura M. Koehly

National Institutes of Health

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