Information for Potential Volunteers

What does ARL do?
The U.S. Army Combat Capabilities Development Command Army Research Laboratory (CCDC ARL) is the nation's premier laboratory for land forces. ARL's mission is to discover, innovate, and transition science and technology to ensure dominant strategic land power.
Why is human research conducted by CCDC ARL?
Research is usually done to answer a question or to determine if one method is better than another. While the research is being done, the answer to the question of which method is better is not known.

Research conducted by ARL employees and contractors ensures that methods, technologies and systems are fully capable of operating during all the tactics, techniques and procedures (TTPs) they will be used for.
What is the Human Research Protection Program?
A. The CCDC ARL Human Research Protection Program (HRPP) provides oversight for all research activities involving human subjects. Before a research study can start, scientists and engineers develop a plan for their research. The plan (protocol or test plan) is first reviewed by the HRPP to determine if the research involves human participants, directly or indirectly. If there is human participation, a review is then conducted by the CCDC ARL Institutional Review Board (IRB).
What is the IRB?
A. The purpose of the CCDC ARL IRB is to ensure the safe and ethical treatment of humans as subjects in research. In accordance with federal and CCDC ARL regulations, it is required that the IRB review all research involving human subjects prior to the initiation of the protocol.

The IRB is made up of scientists, engineers, medical professionals and non-scientists. Its duty is to ensure the protection of people enrolled in research studies. If the IRB does not approve a study, a study cannot start. All studies involving human participants conducted at CCDC ARL must be reviewed and approved by the CCDC ARL IRB.

The Principal Investigator (researcher) is required to return to the IRB any time there is a change and report the progress of the study at least annually. The consent form is reviewed by the IRB to ensure that it contains complete information and that it is written so that it can be understood by people unfamiliar with research terms.

Consent is the first step

  1. You must give voluntary permission in order to participate in a research study. You may not be a participant in a study without your knowledge and consent.
  2. You are under no obligation to participate in any research study. Your decision will not affect any potential benefits you may receive at ARL or from the U.S. Army.
  3. A consent form is long because it is important for you to have all the information needed to make an informed decision. There will be time to answer your questions.
  4. You will receive a copy of the signed consent form after you sign it so that you may refer to it when needed.

The consent process will contain the following:

  • An invitation to be part of the research and who will sponsor the study.
  • An explanation of why the study is being done and a description of the study procedures, including alternative procedures available to you.
  • Information about who may participate in the study.
  • Detailed information on any bad effects (risks and discomforts) as well as any good effects (benefits) that may occur in the study.
  • Identify who will have access to your personal information, how it will be protected and who will be able to use information obtained from the study (including future use of the data).
  • Compensation that may be available.
  • Identify who you may ask for more information about the study or about your rights as a participant in the research study.

Commonly asked questions:

Will I be paid for volunteering?
Sometimes sponsors pay volunteers for their time, information and samples needed for the research. Not all studies pay for participation.
Will I personally benefit if I volunteer?
You will not directly benefit from research conducted by ARL.
What if I am in the military?
Military personnel must inform the Principal Investigator (Pl) of their status. Additional measures will be taken so you can be recruited outside of the chain of command.
What if I don't want to be part of a study?
After you are asked to join and listen to all of the information about the study, YOU decide whether or not you wish to participate. You are under NO obligation to participate in any study.
What if I change my mind?
You may change your mind at any time and leave the study. It will have no effect on your work, command or relationship with CCDC ARL.
Who conducts these research studies?
The Pl has overall responsibility for the study. Study staff may conduct some of the tasks associated with the study, such as making appointments, conducting the consent process and collecting information during the study.

The study staff will closely follow each person enrolled in the study.
Who can I contact if I have more questions?
- The Pl is available to answer questions about the study.
- The CCDC ARL Human Protection Administrator and HRPP office is available to answer questions about your rights as a research subject.

If you would like more information about how research is conducted, how it is overseen, or if you have questions about your rights as a research subject, please contact:


Last Update / Reviewed: September 23, 2019