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1.
Can J Gastroenterol ; 27(12): 717-20, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24340317

ABSTRACT

BACKGROUND: Funders of health research in Canada seek to determine how their funding programs impact research capacity and knowledge creation. OBJECTIVE: To evaluate the impact of a focused grants and award program that was cofunded by the Canadian Institutes of Health Research Institute of Nutrition, Metabolism and Diabetes, and the Canadian Association of Gastroenterology; and to measure the impact of the Program on the career paths of funded researchers and assess the outcomes of research supported through the Program. METHODS: A survey of the recipients of grants and awards from 2000 to 2008 was conducted in 2012. The CIHR Funding Decisions database was searched to determine subsequent funding; a bibliometric citation analysis of publications arising from the Program was performed. RESULTS: Of 160 grant and award recipients, 147 (92%) completed the survey. With >$17.4 million in research funding, support was provided for 131 fellowship awards, seven career transition awards, and 22 operating grants. More than three-quarters of grant and award recipients continue to work or train in a research-related position. Combined research outputs included 545 research articles, 130 review articles, 33 book chapters and 11 patents. Comparative analyses indicate that publications supported by the funding program had a greater impact than other Canadian and international comparators. CONCLUSIONS: Continuity in support of a long-term health research funding partnership strengthened the career development of gastroenterology researchers in Canada, and enhanced the creation and dissemination of new knowledge in the discipline.


Subject(s)
Biomedical Research/economics , Career Choice , Gastroenterology/economics , Publications/statistics & numerical data , Research Support as Topic , Canada , Fellowships and Scholarships , Foundations/economics , Government Agencies/economics , Humans , Public-Private Sector Partnerships , Societies, Medical/economics
2.
Implement Sci ; 7: 57, 2012 Jun 22.
Article in English | MEDLINE | ID: mdl-22726821

ABSTRACT

BACKGROUND: The Canadian Institutes of Health Research (CIHR) has defined knowledge translation (KT) as a dynamic and iterative process that includes the synthesis, dissemination, exchange, and ethically-sound application of knowledge to improve the health of Canadians, provide more effective health services and products, and strengthen the healthcare system. CIHR, the national health research funding agency in Canada, has undertaken to advance this concept through direct research funding opportunities in KT. Because CIHR is recognized within Canada and internationally for leading and funding the advancement of KT science and practice, it is essential and timely to evaluate this intervention, and specifically, these funding opportunities. DESIGN: The study will employ a novel method of participatory, utilization-focused evaluation inspired by the principles of integrated KT. It will use a mixed methods approach, drawing on both quantitative and qualitative data, and will elicit participation from CIHR funded researchers, knowledge users, KT experts, as well as other health research funding agencies. Lines of inquiry will include an international environmental scan, document/data reviews, in-depth interviews, targeted surveys, case studies, and an expert review panel. The study will investigate how efficiently and effectively the CIHR model of KT funding programs operates, what immediate outcomes these funding mechanisms have produced, and what impact these programs have had on the broader state of health research, health research uptake, and health improvement. DISCUSSION: The protocol and results of this evaluation will be of interest to those engaged in the theory, practice, and evaluation of KT. The dissemination of the study protocol and results to both practitioners and theorists will help to fill a gap in knowledge in three areas: the role of a public research funding agency in facilitating KT, the outcomes and impacts KT funding interventions, and how KT can best be evaluated.


Subject(s)
Government Agencies/economics , Health Education/organization & administration , Health Knowledge, Attitudes, Practice , Information Dissemination , Canada , Health Education/economics , Humans
3.
Nurs Leadersh (Tor Ont) ; 20(2): 50-68, 2007.
Article in English | MEDLINE | ID: mdl-17619596

ABSTRACT

The purpose of this study was to examine role structures and processes and their impact on job satisfaction for oncology advanced practice nurses (APNs) in Ontario. APNs caring for adult, paediatric or palliative patients in integrated regional cancer programs, tertiary care hospitals or community hospitals and agencies were invited to complete a mailed self-report questionnaire. A total of 73 of 77 APNs participated in the study. Most APNs (55%) were acute care nurse practitioners employed by regional cancer programs or tertiary care hospitals. Adult patients with breast or haematological cancers and those receiving initial treatment or palliative care were the primary focus of APN roles. APN education needs related to specialization in oncology, leadership and research were identified. Overall, APNs were minimally satisfied with their roles. Role confidence (beta = .404, p = .001) and the number of overtime hours (beta = -.313, p = .008) were respective positive and negative predictors of APN job satisfaction. Progress in role development is described, and recommendations for improving role development and expanding the delivery of oncology APN services are provided.


Subject(s)
Attitude of Health Personnel , Job Satisfaction , Nurse Clinicians/psychology , Nurse Practitioners/psychology , Nurse's Role/psychology , Oncology Nursing , Adult , Certification , Clinical Competence , Education, Nursing, Graduate , Employment/organization & administration , Female , Humans , Male , Middle Aged , Models, Nursing , Nurse Clinicians/education , Nurse Clinicians/organization & administration , Nurse Practitioners/education , Nurse Practitioners/organization & administration , Nursing Methodology Research , Oncology Nursing/education , Oncology Nursing/organization & administration , Ontario , Outcome and Process Assessment, Health Care , Professional Autonomy , Regression Analysis , Self Efficacy , Surveys and Questionnaires , Workload
4.
Int Q Community Health Educ ; 28(2): 127-51, 2007.
Article in English | MEDLINE | ID: mdl-19131305

ABSTRACT

Among those concerned with fighting AIDS worldwide, it is agreed that the best weapon to change people's behavior is education. In this educational effort, all available channels have to be explored. In Ghana, the Health Education Division (HED) of the Ministry of Health set up three drama troupes to carry out AIDS education on a pilot basis. This study evaluates the impact of one of the troupes on AIDS knowledge, attitude and behavior using the focus group research approach. The findings confirm that drama about a well thought out AIDS-related theme does increase knowledge about AIDS and promotes commendable attitudes toward AIDS. It could also lead to changes in sexual behavior. The study also revealed that songs with AIDS-related themes could serve as important cues to "healthful" action in the environment by reminding listeners to adopt safer sexual behaviors.


Subject(s)
Drama , HIV Infections/prevention & control , Health Education/methods , Music , Female , Focus Groups , Ghana , HIV Infections/etiology , HIV Infections/physiopathology , HIV Infections/transmission , Health Knowledge, Attitudes, Practice , Humans , Male , Risk Reduction Behavior
5.
Prog Transplant ; 16(4): 309-16, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17183937

ABSTRACT

BACKGROUND: An increased understanding of the transition process from pediatric to adult transplant care may inform strategies for facilitating the transfer of patients and ultimately improve outcomes of care. OBJECTIVE: To explore the transition process from pediatric to adult transplant care from the perspective of young adults. STUDY DESIGN: Using a qualitative case study approach, data were collected from transplant recipients through organ-specific focus groups, from transplant coordinators and nurse practitioners through interviews, and from electronic documents. Data were analyzed using an editorial format. RESULTS: The analysis identified 5 elements of transition: There to Here, Getting Ready, Frame of Mind, Making It Easier, and Giving Back. In addition, threaded throughout the elements were the themes People Are Important, Expectations of Us, and Information We Need. CONCLUSIONS: The transition for young people from a pediatric to an adult transplant center can be difficult and often traumatic. Young adults who transfer to adult care need to be better prepared for the adult center, made aware of the differences, and introduced to team members before the transfer. Transition programs that aim to improve the transition process should be developed for these patients.


Subject(s)
Adaptation, Psychological , Adolescent Health Services , Attitude to Health , Continuity of Patient Care , Organ Transplantation , Adolescent , Adult , Female , Focus Groups , Humans , Male , Ontario , Organ Transplantation/psychology , Outpatient Clinics, Hospital , Social Support
6.
J Rural Health ; 20(2): 125-30, 2004.
Article in English | MEDLINE | ID: mdl-15085625

ABSTRACT

CONTEXT: Influenza and pneumonia rank among the 5 leading causes of death among persons aged 65 and over. Although immunization has been demonstrated to prevent influenza or reduce its incidence and associated complications among the elderly, it has been largely underutilized. PURPOSE: This study examined the association of attitudes, perceived norms, and intention to obtain influenza immunization among community-dwelling rural elderly. The goal was to design an effective intervention program to increase the rate of flu immunization among the rural elderly. METHODS: In spring 2000, random-digit dialing selected 1,239 households in 2 rural Vermont counties. Telephone interviews were conducted with 799 persons aged 60 or older, resulting in a response rate of 65%. FINDINGS: Factor analyses revealed 2 dimensions underlying attitudes and perceived norms. Subsequent regression analyses confirmed that 1 attitude construct--perceived benefits--and both normative indices were significant predictors of immunization intention, explaining 45% of its variation. CONCLUSIONS: An intervention program targeting rural elderly should emphasize the benefits and perceived side effects of immunization. The program should publicize that most elderly believe that the advantages of influenza immunization outweigh the disadvantages. These findings will inform an intervention program designed to increase immunization coverage among rural seniors in Vermont.


Subject(s)
Health Knowledge, Attitudes, Practice , Health Services Accessibility/statistics & numerical data , Health Services for the Aged/statistics & numerical data , Immunization Programs/statistics & numerical data , Influenza, Human/prevention & control , Needs Assessment , Aged , Aged, 80 and over , Female , Health Care Surveys , Humans , Influenza Vaccines/therapeutic use , Male , Motivation , Regression Analysis , Rural Population/statistics & numerical data , Vermont
7.
Breast J ; 8(6): 338-48, 2002.
Article in English | MEDLINE | ID: mdl-12390356

ABSTRACT

The disablement process model proposed by Nagi in 1965 and subsequently expanded by Verbrugge and Jette was used heuristically to study the relationships among morbidities and arm/shoulder function limitations that breast cancer survivors experience in the period following treatment. A telephone survey was administered to 148 patients (67%) from among 222 breast cancer survivors who had undergone surgery in 1997 and 1998. Sixty-three percent of respondents reported experiencing some numbness, while 35% noticed swelling. Between 13% and 15% reported moderate to severe pain. Similar proportions said the occurrence of pain ranged from intermittent to constant. Between 1% and 4% reported problems with shoulder abduction and flexion and a decrease in arm strength and daily use of the arm. Swellings in the torso and arm tended to cluster into two different factors. Numbness followed a similar pattern. Apart from numbness in the arm, all the other factors had strong significant associations with one another. In multiple regression analyses, current pain intensity and swelling in the arm were independently related to current functional status of the arm/shoulder. The results suggest that it may be feasible to use patients' self-reports to develop a simple lymphedema-specific tool to monitor the functional status of women living with or at risk for lymphedema. Such a tool, if properly designed and implemented, would allow for the timely introduction of lymphedema or pain management strategies to improve arm function and ultimately the quality of life of breast cancer survivors.


Subject(s)
Arm/physiopathology , Breast Neoplasms/surgery , Hypesthesia/etiology , Lymph Node Excision/adverse effects , Lymphedema/etiology , Pain/etiology , Shoulder/physiopathology , Activities of Daily Living , Adult , Aged , Aged, 80 and over , Axilla , Breast Neoplasms/physiopathology , Evaluation Studies as Topic , Female , Humans , Middle Aged , Quality of Life , Regression Analysis , Shoulder Pain/etiology , Statistics, Nonparametric , Surveys and Questionnaires , Survival Analysis , United States , Vermont
8.
Support Care Cancer ; 10(7): 542-8, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12324809

ABSTRACT

This study examined the use of complementary and alternative medicine (CAM) therapies by breast cancer patients and the communication of their CAM use to their physicians relative to lymphedema symptoms and other factors. Breast cancer patients ( N = 148) in the State of Vermont were interviewed 2-3 years after their primary surgery using computer-aided telephone interviewing methods. Questionnaire items included demographic information, treatment, CAM use, lymphedema symptoms, and other measures. A large proportion (72.3%) reported using at least one CAM treatment after surgery. The most frequently used treatments were vitamins and nonfood supplements (72.3%), with herbal treatments, meditation, and traditional massage each being reported by about one-fifth of the women. Age, education, adjuvant chemotherapy, and extremity swelling were associated with use of more CAM treatments in a regression model. A large proportion (73.8%) of CAM users reported their CAM use to their physicians. Correlations between patients' income, adjuvant radiation therapy, and adjuvant tamoxifen use with communication of CAM use to their physicians were sought in a logistic regression model. CAM use is high among breast cancer patients in Vermont, and the number of CAM therapies used is related to demographic factors, adjuvant treatment, and lymphedema symptoms. Communication of CAM use to physicians appears to be multifaceted.


Subject(s)
Breast Neoplasms/therapy , Complementary Therapies/statistics & numerical data , Physicians/statistics & numerical data , Adult , Aged , Aged, 80 and over , Breast Neoplasms/pathology , Communication , Factor Analysis, Statistical , Female , Humans , Logistic Models , Middle Aged , Patient Acceptance of Health Care , Surveys and Questionnaires , Vermont
9.
Patient Educ Couns ; 47(2): 155-63, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12191539

ABSTRACT

Physical therapists, books and oncologist's staff were the most frequently cited sources of lymphedema prevention and management information in a telephone survey of 148 recently treated breast cancer patients. Awareness, current practice and intention to practice 13 recommended prevention behaviors were low, and variations in these indices and in information sources were observed between those reporting any swelling and those who did not. Citing radiation oncologists as an information source reflected significantly higher levels of awareness, practice and intention as compared to not citing them. Also, citing oncologists reflected lower scores on the three indices as compared to not citing them. The results suggest that lymphedema prevention and management information is not getting to breast cancer survivors in a timely fashion and underscore the urgent need to develop and implement appropriate educational strategies. Additionally, research into factors that could motivate survivors to practice the recommended behaviors is warranted.


Subject(s)
Breast Neoplasms/therapy , Health Knowledge, Attitudes, Practice , Lymphedema/prevention & control , Patient Education as Topic , Analysis of Variance , Female , Humans , Lymphedema/etiology , Lymphedema/therapy , Middle Aged , Patient Education as Topic/methods , Patient Education as Topic/standards , Regression Analysis , Surveys and Questionnaires
10.
Prev Med ; 34(6): 567-77, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12052015

ABSTRACT

BACKGROUND: The availability of genetic testing for cancer risk has prompted an examination of the intention of the general public to undergo testing. This study expands a previous psychosocial model of factors influencing intention to undergo genetic testing for cancer in general to the context of colon cancer. METHODS: A sample of 1,836 adult residents of Vermont, New Hampshire, and Maine were interviewed via telephone. The survey instrument included measures derived from the Health Belief Model and additional psychosocial measures adapted from the literature. Structural Equation Modeling techniques were used to examine factors associated with the likelihood to undergo genetic testing. RESULTS: Perceived barriers and benefits of testing, and perceived susceptibility to colon cancer had direct associations with likelihood. Optimism and pessimism had both direct and indirect effects. Age, socioeconomic status, family history, and awareness of genetic testing had indirect effects, and acted through the other factors. The model explained 22% of the variance in likelihood. CONCLUSIONS: Perceived barriers, benefits, susceptibility, optimism, and pessimism directly influenced likelihood, and may also mediate the effect of background factors examined in this study. These findings suggest effective educational strategies to improve decision-making concerning genetic testing for colon cancer risk in the general population.


Subject(s)
Attitude to Health , Colonic Neoplasms/genetics , Data Collection/methods , Genetic Testing/psychology , Adult , Aged , Colonic Neoplasms/psychology , Educational Status , Female , Humans , Maine , Male , Middle Aged , New Hampshire , Social Class , Telephone , Vermont
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