Analysis Of The Internet Survey

Provided to each subject was a consent form to review and sign before their participation in this study. The researcher excluded any identifiable information from the data collection measures. Subjects received a number as they signed in for the information session. The researcher used these numbers to link the subjects to their surveys and their clinical assessments. Their numbers coordinated with the attendance form which was in the sole possession of the researcher. Institution

This provides a guideline that ensures that researchers minimize the amount of risk a study may impose to a participant. When planning a study, it is also important that each of the participants are provided with a sense of security and not placed at a disadvantage. When participants enter into a study, a level of trust is established, and their identities and the information they provide must be protected and never be used against them or exploited for any reason.

This study will not be anonymous as it requires us to collect names for the purpose of completing this research. For the purpose of this study, information will remain confidential. To ensure confidentiality, Non-involving persons or agencies will not have access to information collected to ensure confidentiality.

“Research in health and social care usually relies on obtaining information from individuals using social research methodologies”. (Whitehouse, M, 2010:428). Questionnaires are suitable for obtaining important information from many individuals in a survey who are answering the questions this is known as ‘respondents’. Questionnaires gives us the opportunity to ask questions of participants but also allows answers to be given according to the options constructed by the researcher using a response frame. A response frame allows a limited choice of different responses. Also there are self-completion questions this allows respondents to fill in the answers themselves. The questionnaire may be delivered to individuals directly by hand or by post or even online the researcher may contact through an email address. They may be asked to complete a customer satisfaction questionnaire. For example at college we are sent online questionnaires through are student email, questionnaires

The informed consent should indicate the participant has read, and understands the details of the study. A statement regarding the maintenance of privacy, confidentiality, and right to decline to participate is included on the consent form, and discussed with each participant prior to the beginning of any interviews. One copy of the consent form is provided to the participant for their records, with the original signed copy is maintained by the researcher in safe

Forty surveys were completed successfully which resulted in very conclusive answers. Before conducting the survey all ethical guidelines were followed: a disclaimer was placed at the start of the survey informing participants that all information will remain confidential; the participants privacy will be respected; there will be no lasting harm and the participants will know this is entirely voluntary as the participant has the freedom to refuse or withdraw at any time without

I made an informed consent form. In the informed consent form, I explained the purpose of the study, the methodology of the study and that I will ensure confidentiality by having no identifying information on the questionnaire. None of the participants raised concerns about their rights as a participant. One participant did ask about the purpose of the informed consent.

The potential participant must be given the opportunity to give full consideration regarding the decision whether or not to participate in the research study without undue influence from his or her physician, family, or the scientific investigator. No informed consent may contain any exculpatory language by which the participant waives any legal rights or releases the investigator or sponsor from

Each participant was presented a consent form electronically, and confidentiality was maintained throughout the process. (See Appendix A.) Steps taken to ensure the confidentiality of the respondents included assigning an alias name or number to each respondent requesting such, presenting the consent form that explained to participants that they had been selected to participate in the study, and minimizing “off the record” conversations. The only identification of individual interview data in reports was by subjects’ MASSP

The purpose of this form is to provide you information that may affect you decision as to whether or not to participate in this research study. The person performing the research will answer any of your questions. Please read the information below and ask any questions you might have before deciding whether or not to participate in the study. If you decide to be involved in this study, this form will be used as evidence of consent.

The Belmont Report establishes ethical standards for researchers seeking to involve human subjects (U.S. Department of Health and Human Services, 1979). Among these standards is respect for persons- the right of people to be treated as autonomous agents (U.S. Department of Health and Human Services, 1979). Privacy, anonymity, and confidentiality (PAC) fall under this standard (Farrimond, 2013). In research studies, privacy refers to an expectation that access to participants ' information will be limited to those that have a legitimate right to it (Farrimond, 2013). It is also expected that reasonable steps will be taken to prevent unauthorized access to the information. To expand on privacy, most studies allow anonymity- the removal of names and other identifying information (addresses, job titles, age) to protect the identities of participants (Farrimond, 2013). Anonymity increases the likelihood that potential subjects will agree to participate in a study, as they feel more comfortable disclosing information that may otherwise result in negative consequences (Farrimond, 2013). Confidentiality ensures study participants that their information will not be shared beyond the scope of the study (Farrimond, 2013).

Although the class has not had input into the methodology used to collect the data for this report it is still important for us to know why these methods were used. Questionnaires can be useful in order to get opinions and views from a large groups of people (McLeod 2014), such like conditions for the research for this reports. This can be useful as this can be an easier way of targeting a larger audience other than in interview purposes. This will also be more time consuming as everyone is answering the same questions.

Therefore in order to address this key issue, the author proposes to breif students of the intended research aims at the beginning of a lecture and provide the benefits and potential harms of taking part in the study. Additionally, participants will also be informed of the right to withdraw from the study at anytime without prejudice or impact on their studies. As Dyson & Norrie (2013) recommends the explanation should be carried out in a simplistic way, so that participants can understand and ask questions, in order to provide informed consent. It is important to note as per the RCN (2011) guidelines, at no point will the researcher make the individuals feel pressured or coerced into taking part in this study. The next paragraph will now consider how this carrying out this research is relevent to

Firstly, given the contentious nature of the research topic, it will be vital to ensure all participants are fully briefed regarding the research purpose and scope in order to give their ‘informed consent’ (Brotherton, 2015) before participating in the research.

Although there may be some invasive procedures, care will be taken to limit as many invasive procedures as possible. All personal information shall be de-identified to ensure participation privacy. Any records that contain information that may be construed as sensitive will be inside a locked a cabinet where only researchers directly involved with the study will have access. All computers will be password protected with individual sign-on names that shall be linked to each researcher. To ensure participation is voluntary, every precaution will be taken to make sure potential participants do not feel intimidated or pressured to enter into the study. If a participant appears undecided on their involvement, researchers shall not coerce them into participation in any way.