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Dive into the research topics where Moyez Jiwa is active.

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Featured researches published by Moyez Jiwa.


Preventive Medicine | 2010

How equitable are colorectal cancer screening programs which include FOBTs? A review of qualitative and quantitative studies.

Sara Javanparast; Paul Russell Ward; Graeme P. Young; Carlene Wilson; Stacy M. Carter; Gary Misan; Stephen R. Cole; Moyez Jiwa; George Tsourtos; Angelita Martini; Tiffany K. Gill; Genevieve Baratiny; Michelle Ah Matt

OBJECTIVE To review published literature on the equity of participation in colorectal cancer screening amongst different population subgroups, in addition to identifying factors identified as barriers and facilitators to equitable screening. Studies were included in the review if they included FOBT as at least one of the screening tests. METHOD Relevant published articles were identified through systematic electronic searches of selected databases and the examination of the bibliographies of retrieved articles. Studies of the association with colorectal cancer screening test participation, barriers to equitable participation in screening, and studies examining interventional actions to facilitate screening test participation were included. Data extraction and analysis was undertaken using an approach to the synthesis of qualitative and quantitative studies called Realist Review. RESULTS Sixty-three articles were identified that met the inclusion criteria. SES status, ethnicity, age and gender have been found as predictors of colorectal cancer screening test participation. This review also found that the potential for equitable cancer screening test participation may be hindered by access barriers which vary amongst population sub-groups. CONCLUSION This review provides evidence of horizontal inequity in colorectal cancer screening test participation, but limited understanding of the mechanism by which it is sustained, and few evidence-based solutions.


Journal of Medical Internet Research | 2013

Internet-Based Photoaging Within Australian Pharmacies to Promote Smoking Cessation: Randomized Controlled Trial

Oksana Burford; Moyez Jiwa; Owen Carter; Richard Parsons; Delia Hendrie

Background Tobacco smoking leads to death or disability and a drain on national resources. The literature suggests that cigarette smoking continues to be a major modifiable risk factor for a variety of diseases and that smokers aged 18-30 years are relatively resistant to antismoking messages due to their widely held belief that they will not be lifelong smokers. Objective To conduct a randomized controlled trial (RCT) of a computer-generated photoaging intervention to promote smoking cessation among young adult smokers within a community pharmacy setting. Methods A trial was designed with 80% power based on the effect size observed in a published pilot study; 160 subjects were recruited (80 allocated to the control group and 80 to the intervention group) from 8 metropolitan community pharmacies located around Perth city center in Western Australia. All participants received standardized smoking cessation advice. The intervention group participants were also digitally photoaged by using the Internet-based APRIL Face Aging software so they could preview images of themselves as a lifelong smoker and as a nonsmoker. Due to the nature of the intervention, the participants and researcher could not be blinded to the study. The main outcome measure was quit attempts at 6-month follow-up, both self-reported and biochemically validated through testing for carbon monoxide (CO), and nicotine dependence assessed via the Fagerström scale. Results At 6-month follow-up, 5 of 80 control group participants (6.3%) suggested they had quit smoking, but only 1 of 80 control group participants (1.3%) consented to, and was confirmed by, CO validation. In the intervention group, 22 of 80 participants (27.5%) reported quitting, with 11 of 80 participants (13.8%) confirmed by CO testing. This difference in biochemically confirmed quit attempts was statistically significant (χ2 1=9.0, P=.003). A repeated measures analysis suggested the average intervention group smoking dependence score had also significantly dropped compared to control participants (P<.001). These differences remained statistically significant after adjustment for small differences in gender distribution and nicotine dependence between the groups. The mean cost of implementing the intervention was estimated at AU


Australasian Medical Journal | 2009

Follow-up of breast cancer patients: Preliminary findings from nurse-patient consultations and patient surveys

Moyez Jiwa; Georgia Halkett; Kathleen Deas; Moira O'Connor; Jodie Weir; Catherine O'Driscoll; Elizabeth O'Brien; Lisa Wilson; Sholeh Boyle

5.79 per participant. The incremental cost-effectiveness ratio was AU


BMC Family Practice | 2006

Implementing referral guidelines: lessons from a negative outcome cluster randomised factorial trial in general practice

Moyez Jiwa; Paul Skinner; Akinoso Olujimi Coker; Lindsey Shaw; Michael J. Campbell; Joanne Thompson

46 per additional quitter. The mean cost that participants indicated they were willing to pay for the digital aging service was AU


Health Expectations | 2005

Meeting the educational needs of people at risk of diabetes-related amputation: a vignette study with patients and professionals.

Maxine Johnson; Peggy Newton; Moyez Jiwa; Elizabeth Goyder

20.25 (SD 15.32). Conclusions Demonstrating the detrimental effects on facial physical appearance by using a computer-generated simulation may be both effective and cost-effective at persuading young adult smokers to quit. Trial Registration Australian New Zealand Clinical Trials Registry: ACTRN12609000885291; https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?ACTRN=12609000885291 (Archived by WebCite at http://www.webcitation.org/6F2kMt3kC)


BMC Family Practice | 2014

Unmet needs of patients with chronic obstructive pulmonary disease (COPD): a qualitative study on patients and doctors

Stalia Siew Lee Wong; Nurdiana Abdullah; Adina Abdullah; Su May Liew; Siew Mooi Ching; Ee Ming Khoo; Moyez Jiwa; Yook Chin Chia

BACKGROUND: Although clinicians in both primary and tertiary care settings are involved in the care of breast cancer patients following the active treatment phase, few studies report how patients interact with health care providers.METHODS: Participants in this breast cancer follow-up study were recruited from a hospital based nurse-led follow-up clinic in Western Australia. Methods included audio taped, transcribed consultations with Specialist Breast Nurses (SBNs) and patient self-completed surveys.RESULTS: Preliminary data suggest that SBNs play an important role in supporting women to deal with the impact of breast cancer in the years following active treatment. The data suggest that the process of adjustment to a diagnosis of cancer continues for many years after the treatment has ceased. In many cases the women require on-going support to recalibrate their response to normal physical changes that may or may not be a consequence of surgery, radiotherapy and chemotherapy.


Australian and New Zealand Journal of Public Health | 2011

Equity of colorectal cancer screening: cross‐sectional analysis of National Bowel Cancer Screening Program data for South Australia

Paul Russell Ward; Sara Javanparast; Michelle Ah Matt; Angelita Martini; George Tsourtos; Stephen R. Cole; Tiffany K. Gill; Paul Aylward; Genevieve Baratiny; Moyez Jiwa; Gary Misan; Carlene Wilson; Graeme P. Young

BackgroundFew patients with lower bowel symptoms who consult their general practitioner need a specialist opinion. However data from referred patients suggest that those who are referred would benefit from detailed assessment before referral.MethodsA cluster randomised factorial trial. 44 general practices in North Trent, UK. Practices were offered either an electronic interactive referral pro forma, an educational outreach visit by a local colorectal surgeon, both or neither. The main outcome measure was the proportion of cases with severe diverticular disease, cancer or precancerous lesions and inflammatory bowel disease in those referred by each group. A secondary outcome was a referral letter quality score. Semi-structured interviews were conducted to identify key themes relating to the use of the softwareResultsFrom 150 invitations, 44 practices were recruited with a total list size of 265,707. There were 716 consecutive referrals recorded over a six-month period, for which a diagnosis was available for 514. In the combined software arms 14% (37/261) had significant pathology, compared with 19% (49/253) in the non-software arms, relative risk 0.73 (95% CI: 0.46 to 1.15). In the combined educational outreach arms 15% (38/258) had significant pathology compared with 19% (48/256) in the non-educational arms, relative risk 0.79 (95% CI: 0.50 to 1.24). Pro forma practices documented better assessment of patients at referral.ConclusionThere was a lack of evidence that either intervention increased the proportion of patients with organic pathology among those referred. The interactive software did improve the amount of information relayed in referral letters although we were unable to confirm if this made a significant difference to patients or their health care providers. The potential value of either intervention may have been diminished by their limited uptake within the context of a cluster randomised clinical trial. A number of lessons were learned in this trial of novel innovations.


Journal of Radiotherapy in Practice | 2010

Effective Communication and Information Provision in Radiotherapy - The Role of Radiation Therapists

Georgia Halkett; Susan Merchant; Moyez Jiwa; Michala Short; Hayley Arnet; Sharon Richardson; Rachel Kearvell; Sharron Carson; Nigel Spry; Mandy Taylor; Linda J. Kristjanson

Objective  To investigate how patients and professionals view the role of advice in diabetes foot care, in order to inform educational practice.


Journal of Palliative Medicine | 2011

The Palliative Care Interdisciplinary Team: Where Is the Community Pharmacist?

Moira O'Connor; Judith Pugh; Moyez Jiwa; Jeff Hughes; Colleen Fisher

BackgroundChronic Obstructive Pulmonary Disease (COPD) is a chronic disease with repeated exacerbations resulting in gradual debilitation. The quality of life has been shown to be poor in patients with COPD despite efforts to improve self-management. However, the evidence on the benefit of self-management in COPD is conflicting. Whether this could be due to other unmet needs of patients have not been investigated. Therefore, we aimed to explore unmet needs of patients from both patients and doctors managing COPD.MethodsWe conducted a qualitative study with doctors and patients in Malaysia. We used convenience sampling to recruit patients until data saturation. Eighteen patients and eighteen doctors consented and were interviewed using a semi-structured interview guide. The interviews were audio-recorded, transcribed verbatim and checked by the interviewers. Data were analysed using a thematic approach.ResultsThe themes were similar for both the patients and doctors. Three main themes emerged: knowledge and awareness of COPD, psychosocial and physical impact of COPD and the utility of self-management. Knowledge about COPD was generally poor. Patients were not familiar with the term chronic obstructive pulmonary disease or COPD. The word ‘asthma’ was used synonymously with COPD by both patients and doctors. Most patients experienced difficulties in their psychosocial and physical functions such as breathlessness, fear and helplessness. Most patients were not confident in self-managing their illness and prefer a more passive role with doctors directing their care.ConclusionsIn conclusion, our study showed that knowledge of COPD is generally poor. There was mislabelling of COPD as asthma by both patients and physicians. This could have resulted in the lack of understanding of treatment options, outcomes, and prognosis of COPD. The misconception that cough due to COPD was contagious, and breathlessness that resulted from COPD, had important physical and psychosocial impact, and could lead to social isolation. Most patients and physicians did not favour self-management approaches, suggesting innovations based on self-management may be of limited benefit.


International Journal of Family Medicine | 2011

Developing a Self-Administered Questionnaire as a Guide to Consultations with Women Treated for Breast Cancer

Moyez Jiwa; Wendy Chan She Ping-Delfos; Kathy Briffa; Jill Sherriff; Gareth Merriman; Janice Nockolds; Liz Jardine; Toni Musiello; Glenys Longman

Objective: The National Bowel Cancer Screening Program (NBCSP) is a population‐based screening program based on a mailed screening invitation and immunochemical faecal occult blood test. Initial published evidence from the NBCSP concurs with international evidence on similar colorectal cancer screening programs about the unequal participation by different population sub‐groups. The aim of the paper is to present an analysis of the equity of the NBCSP for South Australia, using the concept of horizontal equity, in order to identify geographical areas and population groups which may benefit from targeted approaches to increase participation rates in colorectal cancer screening.

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L. Burridge

University of Queensland

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Afaf Girgis

University of New South Wales

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R. Hodder

Sir Charles Gairdner Hospital

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