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Friday, September 30, 2011

Market Research Focus Groups Service

Group interviews and group discussions are known as Focus groups. They are used to understand the position or behavior of the interviewer or audience. At the time of Focus Groups Six to twelve individuals are selected and either one or two moderators are selected for conduct successful Focus Groups. If they are having two moderators, they will be adopting opposite positions. The moderator is those who introduce the topic. Market research focus groups discussion are controlled through these moderators. These market research focus groups are watched from adjacent rooms. There are various devices used to record these discussions.
Four basic steps to conducting successful focus groups:
  • Planning
  • Recruiting
  • Moderating
  • Analysis and Reporting
Planning
The Successful focus group requires good planning.
  • The site should be ready to access easily.
  • The site should be large enough to accommodate the group and moderator, but not so large that participant’s feel uncomfortable.
  • Participants should see and hear one another during the group.
Recruiting
Focus group respondents are important to have a diverse group, even if respondents all fall under the same group of selection criteria. Example, you might want to recruit a group of patients, within the group of patients, you should be have a  diverse a group as possible in order to learn as much as, at least you can about the attitudes, perceptions, and beliefs of as many types of patients.
Moderating
A focus groups moderator can make a break in focus group. If possible, you can use an experienced moderator. If you should not unable to do this, at least keep the following in mind when selecting someone use to moderate the group:
  • Person should have well at drawing people out and encouraging people to speak.
  • Person should able to control overly dominant people or people making inappropriate comments without disrupting the group.
  • Person should be able to ask all of the predetermined questions, but also follow up on comments made by respondent that needs clarification.
Signed Releases
This is a good idea to get a signed release from focus group participants. While you should protect their identities, you want permission to use their opinions as direct quotes but you also want to spell out for them the conditions of their participation. If you are paying participants a fee for their participation you should also have them sign a form indicating that they received an incentive in whatever amount you determine for their participation in the focus group (this is important to create an audit trail).
Need for Successful Focus Groups
  • Pens
  • Chart Paper
  • Easel
  • Moderator
  • Note taker
  • Tape recorder
Analysis and Reporting
The way that focus groups data is analyzed and reported varies greatly. If you are the person writing the report, it is important to attend the groups if at all possible, or to transcribe the tapes from the group in order to really understand the degree of feeling people used while expressing their ideas. It is a good idea to write up the group as soon after it occurs as possible, while it is still fresh in your mind.
Costs to Plan for Focus Groups:
  • Site
  • Moderator
  • Recruitment fees
  • Participant stipends
  • Other participant costs
  • Translation
  • Transcription

Monday, September 19, 2011

Clinical Trial Software Case Report Form

A Case Report Form is an electronic or paper questionnaire specifically used in clinical trial research. The Case Report Form is the tool used to sponsor of the clinical trial to collect data from each participating site. All data on each patient participating in a clinical trial are held documented in CRF. The sponsor of the clinical trial develops use the CRF to collect specific data, they need in order to test their hypotheses or answer their research questions. The size of the CRF range from handwritten one-time snapshot of a patient's physical condition to hundreds of pages in electronically captured data obtained over a period of weeks or months. It can also include all the required check-up and visits months after the patient's treatment has stopped.
The sponsor is responsible for all the designing of CRF that accurately represents the protocol of clinical trial, and managing its production, monitoring the data collection and auditing the content are filled-in CRF. Case report form contains all the data obtained during the patient's participation in clinical trial. Before sent to the sponsor, this data is usually de-identified that is not traceable to the patient, by removing the patient's name, medical record number, etc., and giving the patient unique study number. The monitoring oversees the release of any personally identifiable data to the sponsor by Institutional Review Board (IRB).
The main logistic goal of a clinical trial is to be obtaining accurate CRF from sponsor's point. Because of human and machine error, the data entered in CRF is rarely completely accurate or entirely readable. When the study of administrators or automated mechanisms processes the CRF, it was sent to the sponsor by local researchers, they use to make a note of queries. Queries are non-sensible or questionable data that must be explained.
Case report form should be built for:
  • Gather all the accurate information that answer study questions, and is consistent with study protocol.
  • Organize and label forms and fields so that data entry is non-rational.
  • Avoid the duplication of data.
Reasons for Standard case report form templates:
  • Eliminate Form Duplication: Some of the data requirements are same across studies, such as demographics, admission checklists, concomitant medications, and adverse events. This is especially true for organizations that carry out multiple studies in the same research area.
  • Simplify Creating New Case Report Forms: There is no need to start from scratch, templates can be customized.
  • Reduce the Data Entry Learning Curve: Templates are using the same visual style and basic organization become familiar to entering data, reducing the data entry learning curve.

Thursday, September 15, 2011

Data Collection Research Methods and Techniques

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