- About the Study
You are being asked to participate in a research study. Taking part in this study is voluntary. The investigators will explain the study to you and will any answer any questions you might have. It is your choice whether or not you take part in this study. If you agree to participate and then choose to withdraw from the study, that is your right, and your decision will not be held against you.
This research study examines context data on mobile phones of users in the real world. This data will assist in the development of new software testing techniques that we anticipate will help to improve the quality of mobile applications.
You are being asked to take part in a research study about the context data patterns of mobile phone users. This involves the collection of date regarding the occurrence of context events (e.g. changes in network availability, battery power levels, location, plugging and unplugging input and output devices, etc.) from your mobile phone. The collected data will be used to determine real-world sequences of context events that could potentially affect the functionality and testing of mobile applications.
Your participation in this research study involves installing an app and letting it run so that it sends us data about the context changes that occur on your phone. More details will be provided in the next section.
You will be asked to install an application on your phone that would run non-intrusively in the background all through the one-month duration of the study. The app will collect data gathered from
You might want to participate in this study if you want to help improve the general reliability and efficiency of mobile applications built for Android phones. The data is expected to be used for research within UNT and external organizations to advance their applications and testing processes. However, you might not want to participate in this study if you are unwilling to keep the app installed on your phone for a one-month period.
You may choose to participate in this research study if you are a mobile phone user and 18 years old or older.
The reasonable foreseeable risks or discomforts to you if you choose to take part is Possible reduction in battery life and increase in device memory usage. You will not receive compensation for participation.
- Details of the Study
DETAILED INFORMATION ABOUT THIS RESEARCH STUDY:The following is more detailed information about this study, in addition to the information listed above.
PURPOSE OF THE STUDY:This study collects context data from phones so that we may better understand real world context patterns and incorporate them into testing with the aim to improve the quality of mobile applications.
TIME COMMITMENT:Participants will install the context data collection app which takes approximately 5 minutes. Participants will let this app run in the background of their phone for one month.
STUDY PROCEDURES:Participants will download and install the data collection app. They will then let the app run in the background of their mobile device for one month. The app will automatically upload the data to our server.
You will be asked to install an application on your phone that would run non-intrusively in the background all through the one-month duration of the study. The app will collect data gathered from
POSSIBLE BENEFITS:This study is expected to produce vital information and insight that may affect the thoroughness of testing processes for mobile applications. It is hoped that your contributions is expected to help improve the general reliability and efficiency of mobile applications built for Android phones. The data is expected to be used for research within UNT and external organizations to advance their applications and testing processes.
POSSIBLE RISKS/DISCOMFORTS:Possible reduction in battery life and increase in device memory usage.
If you experience excessive discomfort when completing the research activity, you may choose to stop participating at any time without penalty. The researchers will try to prevent any problem that could happen, but the study may involve risks to the participant, which are currently unforeseeable. UNT does not provide medical services, or financial assistance for emotional distress or injuries that might happen from participating in this research. If you need to discuss your discomfort further, please contact a mental health provider, or you may contact the researcher who will refer you to appropriate services. If your need is urgent, helpful resources include [provide relevant 24 hour resource information and campus or community resources.
Remember that you have the right to withdraw any study procedures at any time without penalty, and may do so by informing the research team.
This research study is not expected to pose any additional risks beyond what you would normally experience in your regular everyday life. However, if you do experience any discomfort, please inform the research team at Renee[dot]Bryce[at]unt[dot]edu
COMPENSATION: There is no compensation for this study.
CONFIDENTIALITY: Your name will only exist on this consent form and nowhere else. All other data collected during this experiment will be linked to a numerical ID. Your name will not be associated or distributed with the data set.. This consent form will be maintained in a locked file cabinet and will be destroyed three years after the end of the study. These non-identifiable records may be released to others in the future.
We anticipate that your data will be part of a public dataset and/or licensed to companies in the future. The results of this study may be published and/or presented without naming you as a participant. The data collected about you for this study will be used for future research studies that are not described in this consent form. If that occurs, an IRB would first evaluate the use of any information that is identifiable to you, and confidentiality protection would be maintained.
While absolute confidentiality cannot be guaranteed, the research team will make every effort to protect the confidentiality of your records, as described here and to the extent permitted by law. In addition to the research team, the following entities may have access to your records, but only on a need-to-know basis: the U.S. Department of Health and Human Services, the FDA (federal regulating agencies), the reviewing IRB, and sponsors of the study.
CONTACT INFORMATION FOR QUESTIONS ABOUT THE STUDY If you have any questions about the study you may contact Renee[dot]Bryce[at]unt[dot]edu. Any questions you have regarding your rights as a research subject, or complaints about the research may be directed to the Office of Research Integrity and Compliance at 940-565-4643, or by email at untrib[at]unt[dot]edu.
CONSENT:
- Your signature below indicates that you have read, or have had read to you all of the above.
- You confirm that you have been told the possible benefits, risks, and/or discomforts of the study
- You understand that you do not have to take part in this study and your refusal to participate or your decision to withdraw will involve no penalty or loss of rights or benefits.
- You understand your rights as a research participant and you voluntarily consent to participate in this study; you also understand that the study personnel may choose to stop your participation at any time.
- By signing, you are not waiving any of your legal rights.
- People
- Farhan Rahman Arnob, FarhanRahmanArnob[at]my[dot]unt[dot]edu
- Rubel Hassan Mollik, RubelHassanMollik[at]my[dot]unt[dot]edu
- Jarin Tasnim Ishika, JarinTasnimIshika[at]my[dot]unt[dot]edu