scholarly journals Women Who Have Sex with Women’s Attitudes and Willingness to Participate in Future Female Same Sex Public Health Research: Opportunity for Disease Prevention and Control in Tanzania

2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Switbert R Kamazima ◽  
Happiness P Saronga ◽  
Saidah S Bakar ◽  
Jackline V Mbishi

Recruitment of acceptable number of participants in a (public) health research with ‘hard to reach’/‘hidden’ populations is an old global problem, mostly challenging public health researchers in resource limited countries like Tanzania. Violence, stigma, criminalization of behaviors practiced by these groups, and potential participants’ suspicion toward the research and the researchers, further limit willingness to voluntarily participate. We conducted a cross-sectional descriptive and retrospective qualitative formative study with women who have sex with women in Dar-es-Salaam City region, Tanzania. The aim, among other objectives, was to understand women who have sex with women’s attitudes and willingness to participate in future female same sex public health research targeting this group. Findings indicate that all women we studied expressed willingness to participate in future health research targeting issues around female same sex relationships in the Tanzania context; an opportunity for (public) health professionals to prevent and control diseases in the country. To attain this goal, we recommend tailoring research protocols’ content, communication messages, and recruitment tactics to recognize, appreciate, and embrace the specific characteristics, backgrounds, and concerns of women who have sex with women in Tanzania.

2021 ◽  
pp. 47-58
Author(s):  
Manolis Kogevinas ◽  
Leda Chatzi

This chapter will first describe the uses of cross-sectional studies in epidemiological and public health research and then discuss methodological issues concerning the design, the main biases of these studies including response rates, and how to improve participation. In recent years these studies have also incorporated the collection of biospecimens. In aetiological research, cross-sectional studies are suitable epidemiological means for studying non-fatal diseases and effects on physiological variables that do not have a clear time of onset. However, the design of cross-sectional studies makes them less appropriate than other study designs for investigating causal associations. The chapter will finally discuss issues related to the statistical analysis of cross-sectional studies. Many of these issues are also relevant to other epidemiological designs.


2015 ◽  
Vol 3 (10) ◽  
pp. 1-152 ◽  
Author(s):  
Simon C Moore ◽  
Mohammed Fasihul Alam ◽  
David Cohen ◽  
Kerenza Hood ◽  
Chao Huang ◽  
...  

BackgroundViolence in and around premises licensed for the on-site sale and consumption of alcohol continues to burden the NHS with assault-related injuries.Trial designA randomised controlled trial with licensed premises as the unit of allocation, with additional process and cost-effectiveness evaluations.MethodsPremises were eligible (n = 837) if they were licensed for on-site sale and consumption of alcohol, were within 1 of the 22 local authorities (LAs) in Wales and had previously experienced violence. Data were analysed using Andersen–Gill recurrent event models in an intention-to-treat analysis. An embedded process evaluation examined intervention implementation, reach, fidelity, dose and receipt. An economic evaluation compared costs of the intervention with benefits.InterventionPremises were randomised to receive a violence-reduction intervention, Safety Management in Licensed Environments (SMILE), which was delivered by an environmental health practitioner (EHP; the agent). SMILE consisted of an initial risk audit to identify known risks of violence, a follow-up audit scheduled to enforce change for premises in which serious risks had been identified, structured advice from EHPs on how risks could be addressed in premises and online materials that provided educational videos and related material.ObjectiveTo develop intervention materials that are acceptable and consistent with EHPs’ statutory remit; to determine the effectiveness of the SMILE intervention in reducing violence; to determine reach, fidelity, dose and receipt of the intervention; and to consider intervention cost-effectiveness.OutcomeDifference in police-recorded violence between intervention and control premises over a 455-day follow-up period.RandomisationA minimum sample size of 274 licensed premises per arm was required, rounded up to 300 and randomly selected from the eligible population. Licensed premises were randomly assigned by computer to intervention and control arms in a 1 : 1 ratio. Optimal allocation was used, stratified by LA. Premises opening hours, volume of previous violence and LA EHP capacity were used to balance the randomisation. Premises were dropped from the study if they were closed at the time of audit.ResultsSMILE was delivered with high levels of reach and fidelity but similar levels of dose to all premises, regardless of risk level. Intervention premises (n = 208) showed an increase in police-recorded violence compared with control premises (n = 245), although results are underpowered. An initial risk audit was less effective than normal practice (hazard ratio = 1.34, 95% confidence interval 1.20 to 1.51) and not cost-effective. Almost all eligible intervention premises (98.6%) received the initial risk audit; nearly 40% of intervention practices should have received follow-up visits but fewer than 10% received one. The intervention was acceptable to EHPs and to some premises staff, but less so for smaller independent premises.ConclusionsSMILE was associated with an increase in police-recorded violence in intervention premises, compared with control premises. A lack of follow-up enforcement visits suggests implementation failure for what was seen as a key mechanism of action. There are also concerns as to the robustness of police data for targeting and assessing outcome effectiveness, while intervention premises may have received greater attention from statutory agencies and, therefore, the identification of more violence than control premises. Although SMILE had high reach and was feasible and acceptable to EHPs, it was found to be ineffective and associated with increased levels of violence, compared with normal practice and it requires additional work to promote the implementation of follow-up enforcement visits. Future work will aim to better understand the role of intervention dose on outcomes and seek more objective measures of violence for use in similar trials.Trial registrationCurrent Controlled Trials ISRCTN78924818.FundingThis project was funded by the NIHR Public Health Research programme and will be published in full inPublic Health Research; Vol. 3, No. 10. See the NIHR Journals Library website for further project information.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Michelle Amri ◽  
Christina Angelakis ◽  
Dilani Logan

Abstract Objective Through collating observations from various studies and complementing these findings with one author’s study, a detailed overview of the benefits and drawbacks of asynchronous email interviewing is provided. Through this overview, it is evident there is great potential for asynchronous email interviews in the broad field of health, particularly for studies drawing on expertise from participants in academia or professional settings, those across varied geographical settings (i.e. potential for global public health research), and/or in circumstances when face-to-face interactions are not possible (e.g. COVID-19). Results Benefits of asynchronous email interviewing and additional considerations for researchers are discussed around: (i) access transcending geographic location and during restricted face-to-face communications; (ii) feasibility and cost; (iii) sampling and inclusion of diverse participants; (iv) facilitating snowball sampling and increased transparency; (v) data collection with working professionals; (vi) anonymity; (vii) verification of participants; (viii) data quality and enhanced data accuracy; and (ix) overcoming language barriers. Similarly, potential drawbacks of asynchronous email interviews are also discussed with suggested remedies, which centre around: (i) time; (ii) participant verification and confidentiality; (iii) technology and sampling concerns; (iv) data quality and availability; and (v) need for enhanced clarity and precision.


2017 ◽  
Vol 1 ◽  
pp. 89-89 ◽  
Author(s):  
Donna F. Stroup ◽  
C. Kay Smith ◽  
Benedict I. Truman

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