Medical research protocol

And ch policy ended format for a research the abstract of a research paper, the project summary, should be no more than 300 words and at the most a page long (font size 12, single spacing). Provided preferably on a separate page, it should summarize all the central elements of the protocol, for example the rationale, objectives, methods, populations, time frame, and expected outcomes. It should stand on its own, and not refer the reader to points in the project ol title, protocol identifying number (if any), and and address of the sponsor/ and title of the investigator(s) who is (are) responsible for conducting the research, and the address and telephone number(s) of the research site(s), including responsibilities of (s) and address(es) of the clinical laboratory(ies) and other medical and/or technical department(s) and/or institutions involved in the ale & background rationale specifies the reasons for conducting the research in light of current knowledge. It is the equivalent to the introduction in a research paper and it puts the proposal in context.

It should answer the question of why and what: why the research needs to be done and what will be its relevance. They create a setting for the ic objectives are statements of the research question(s). Objectives should be simple (not complex), specific (not vague), and stated in advance (not after the research is done). The design of the study should include information on the type of study, the research population or the sampling frame, and who can take part (e.

For example, a study may be described as being a basic science research, epidemiologic or social science research, it may also be described as observational or interventional; if observational, it may be either descriptive or analytic, if analytic it could either be cross-sectional or longitudinal etc. The link below provides more information on how to describe a research methodology section is the most important part of the protocol. If multiple sites are engaged in a specified protocol, methodology should be standardized and clearly entions should be described in detail, including a description of the drug/device/vaccine that is being tested. Interventions could also be in the realm of social sciences for example providing training or information to groups of ures could be biomedical (collection of blood or sputum samples to develop a diagnostic test), or in the realm of social sciences (doing a questionnaire survey, carrying out a focus group discussion as part of formative research, observation of the participant's environment, etc.

Safety aspects of the research should always be kept in mind and information provided in the protocol on how the safety of research participants will be ensured. It is useful to remember that even administering a research questionnaire can have adverse effects on research protocol must give a clear indication of what follow up will be provided to the research participants and for how long. This may include a follow u, especially for adverse events, even after data collection for the research study is management and statistical protocol should provide information on how the data will be managed, including data handling and coding for computer analysis, monitoring and verification. For projects involving qualitative approaches, specify in sufficient detail how the data will be protocol should describe the quality control and quality assurance system for the conduct of the study, including gcp, follow up by clinical monitors, dsmb, data management ed outcomes of the protocol should indicate how the study will contribute to advancement of knowledge, how the results will be utilized, not only in publications but also how they will likely affect health care, health systems, or health ination of results and publication protocol should specify not only dissemination of results in the scientific media, but also to the community and/ or the participants, and consider dissemination to the policy makers where relevant.

Publication policy should be clearly discussed- for example who will take the lead in publication and who will be acknowledged in publications, on of the protocol should specify the time that each phase of the project is likely to take, along with a detailed month by month timeline for each activity to be section should discuss the difficulties that the investigators anticipate in successfully completing their projects within the time frame stipulated and the funding requested. It should also offer possible solutions to deal with these section should describe the role and responsibility of each member of the protocol should have a description of ethical considerations relating to the study. It should also describe how the investigator(s) plan to obtain informed consent from the research participants (the informed consent process). Consent approved version of the protocol must have copies of informed consent forms (icf), both in english and the local language in which they are going to be administered.

If the research involves more than one group of individuals, for example healthcare users and healthcare providers, a separate specifically tailored informed consent form must be included for each group. For guidance on how to write an informed consent form, click mmes and region of the south-east asia eastern mediterranean western pacific up for who the browser controls to adjust the font size, or print this al research tion - clinical research protocols (protocols) are research studies conducted by nih staff. A drug or medical device, or may review previous studies or record the history of a disease or condition. Staff on a protocol consist of a principal investigator (pi), possibly a co-principal investigator (co-pi), one or several associate investigators (ai), a medical advisory investigator (mai), and a research contact (rc).

To protect the integrity of the protocol and therefore the nih in general, the financial interests of the nih employees named on a protocol must be reviewed to confirm that no conflict of interest exists between investigators’ official duties on the protocol and their personal or imputed financial form 717-1: confidential report of financial interests in substantially affected organizations for employees of the national institutes of ated with authoring office and date. Guide to avoiding financial and non-financial conflicts or perceived conflicts of interest in clinical research at nih(oir/cc, updated 10/14) (pdf, 6 pages). Links policy for data and safety monitoring of human subject research safety and monitoring board , you need to enable javascript for this page to function research g trials, grant proposals, formative research, methods, early our readers and authors are saying:This theme's latest ed jmir sister theme's latest submission open for ctive simulation of liver biopsy puncture training procedures: combining immersive virtual reality anatomy learning mode with integrated haptic ound: educational methodologies for training surgeons and radiologists has not significantly changed over recent years. This could be extended to numerous competency based clinical procedural training scenarios in the submitted: oct 31, 2017 open peer review period: oct 31, 2017 - nov 14, research protocols is open for nominations for section editors and an you interested in research methods?

Do you have a special interest in research ethics and integrity of research, and do you see the importance of prospectively publishing research protocols? Research protocols (issn 1929-0748) publishes peer-reviewed, openly accessible research ideas and grant proposals, study and trial protocols, reports of ongoing research, current methods and approaches, and preliminary results from pilot studies or formative research informing the design of medical and health-related research and technology res protoc is a new journal spin-off of jmir, the worlds' leading medical journal in health sciences / health services research and health informatics (impact factor 2016: 5. Res protoc publishes protocols and grant proposals in all areas of medicine (and their peer-review reports, if available), as well as feasibility studies, early reports and formative/process evaluations of ongoing studies and descriptions of the development and pilot evaluations of innovations and software applications or other res protoc is fully open access, with full text articles deposited in pubmed hing research protocols, grant proposals, pilot/feasibility studies and early reports of ongoing and planned work encourages collaboration and early feedback, and reduces duplication of res protoc will be a valuable ressource for researchers who want to learn about current research methodologies and how to write a winning grant res protoc creates an early scientific record for researchers who have developed novel methodologies, software, innovations or elaborate res protoc faciliates subsequent publication of results demonstrating that the methodology has already been reviewed, and reduces the effort of writing up the results, as the protocol can be easily res protoc demonstrates to reviewers of subsequent results papers that authors followed and adhered to carefully developed and described a-priori s whose protocols or grant proposal have been accepted in jmir res protoc are "in principle accepted" for subsequent publication of results in other jmir journals as long as authors adhere to their original protocol - regardless of study results (even if they are negative), reducing publication bias in s publishing their protocols in jmir res protoc will receive a 20% discount on the article processing fee if they publish their results in another journal of the jmir journal family (for example, jmir for ehealth studies, i-jmr for others). Incentives alone versus incentivized partner support for promoting smoking cessation during pregnancy and postpartum: protocol for a non-randomized...

Te d’ivoire dual burden of disease (codubu): study protocol to investigate the co-occurrence of chronic infections and noncommunicable diseases in rural... Validation study of first trimester obstetric prediction models (expect study i): research protocol and population jacqueline elisabeth ina cj ne j res protoc 2017;6(10): one of the following formats:Or, copy the article link to your clipboard:Bibtexfor: bibdesk and : refman, procite, endnote, this article to your mendeley this article to your citeulike citation to er social media mentions by hovering over the donut. Delivered dialectical behavioral therapy skills training for suicidal and heavy episodic drinkers: protocol and preliminary results of a randomized... Adoption of social media to recruit participants for the cool runnings randomized controlled trial in ound: using social media to recruit specific populations for research studies is gaining popularity.

Of hepatitis c virus among people who inject drugs: protocol for a systematic review and res protoc 2017;6(10): one of the following formats:Or, copy the article link to your clipboard:Bibtexfor: bibdesk and : refman, procite, endnote, this article to your mendeley this article to your citeulike citation to er social media mentions by hovering over the donut. Challenge-based approach to body-weight supported treadmill training poststroke: study protocol for a randomized control submitted: oct 30, peer review period: oct 31, 2017 - nov 14, ound: body weight support (bws) treadmill training protocols in conjunction with other modalities are commonly used to improve poststroke balance and walking function. Body weight support (bws) treadmill training protocols in conjunction with other modalities are commonly used to improve poststroke balance and walking function. Objective: we describe two unique bws treadmill training protocols of similar training intensity that integrated dynamic-balance challenges, to help improve ambulatory function poststroke.

Results: *no results* conclusions: these treadmill-training protocols represent advances in standardized approaches to selecting bws levels without the necessity for using handrails or manual assistance, to progressively provide dynamic-challenges for improving poststroke ambulatory function. Prospective study to investigate the diagnostic accuracy of reflectance confocal microscopy to diagnose skin cancer: research submitted: oct 30, peer review period: oct 31, 2017 - nov 14, cancer is the most common type of cancer in the uk, with over 100,000 cases diagnosed each year. Results: the protocol of this study was approved by the medical ethics committee of vu university medical center and the competent authority (ccmo). Clinical trial: social media and online networking to develop the geriatric medicine research collaborative (gemrc), united submitted: oct 30, peer review period: oct 30, 2017 - nov 13, ional pathways to promote collaboration between researchers typically take years to expand beyond individual institutions.

Social media and online networking provides an innovative approach to the development and promotion of collaborative research projects. We present the formation and development of the geriatric medicine research collaborative (gemrc), united kingdom; a new national trainee-led research collaborative. The aims of this collaborative are to facilitate research projects that will directly benefit older patients, improve research skills of geriatric medicine trainees, and to facilitate recommendations for healthcare policy for older methods of collaboration are described; trainee-led meetings regionally, and at national conferences, e-mail communication, direct uploading of project material to our website, social media, and virtual meetings. The utilization of virtual communication has potential to lead to international, as well as national, collaborations, and lead to research that improves outcomes for older s games to improve genetic literacy and genetic risk awareness in the general public: protocol for usability and knowledge transfer submitted: oct 27, peer review period: oct 29, 2017 - nov 12, manuscript needs more ound: genetic testing and genetic risk information are gaining importance in the context of personalized medicine and disease prevention.

If the proposed games will be able to improve users’ knowledge, we will reach the educational imperative of the “genetic era”: improving genetic literacy in the general , you need to enable javascript for this page to function research g trials, grant proposals, formative research, methods, early our readers and authors are saying:This theme's latest ed jmir sister theme's latest submission open for ctive simulation of liver biopsy puncture training procedures: combining immersive virtual reality anatomy learning mode with integrated haptic ound: educational methodologies for training surgeons and radiologists has not significantly changed over recent years.