The Donor Conception Network (DCN) receives many requests from researchers asking if they can approach members of the DCN to take part in their research. As we have a duty to protect the interests of our members, we have set up this web page to enable you to become more familiar with the research procedure.
The research procedure consists of 6 key steps which sets out the process and timings of the research application procedure. All research applications are reviewed by our specialist research advisors who consider all applications undertaking research involving our members. The 6 key steps are described below:
What steps do I need to take to carry out research within DCN?
1. Ensure you have read the research policy, you can read it on this page or download it here -
3. Complete the Checklist and append all requested documentation. Send your completed application and supporting documents to email@example.com
4. The DCN requires up to 30 days to review the checklist and submitted research documentation and provide a response; this can be approval for the research to take place under the auspices of the DCN, a request for amendments or further information or a rejection.
5. Once your application has been reviewed and we have approved it, we will circulate the research request (via email) to our members (or target it to specific groups) to support your research.
6. Further down the line, we ask that you report back to DCN the outcomes of your research (including the response rate from DCN members) and references or copies of any resulting publications. We would like to place a summary of the work done on our website.
This information is important if:
You wish to conduct a piece of research involving members of the DCN (please note the DCN research group require a minimum of 30 days’ notice to review a proposal)
You have been asked to participate in a research project
Donor Conception Network research policy statement The DCN recognises that research is a valuable tool for learning, empowerment, and improving services for:
parents with children conceived with donated gametes
people contemplating or undergoing treatment
The aims of this policy are to ensure that all research undertaken within the DCN:
promotes best practice in research and research-related activity
contributes to genuinelyevidence-based policy
safeguards the dignity, rights, safety and well-being of participants as the primary consideration for all research studies and helps to avoid unacceptable risk to the researchers
promotes equality in line with the Equality Act 2010 (which identifies discrimination as unlawful if it is based on: age, disability, gender reassignment, marriage and civil partnership, pregnancy, maternity, race, religion or belief, sex, sexual orientation)
adheres todata protection requirements
promotes efficiency and reduction of ‘consultation fatigue' by avoiding where possible duplication of research activity (i.e.. a project is less likely to be approved by the research committee if a similar one has recently been undertaken)
improves dissemination of current and future research findings
ensuresfree and comprehensive access to information on research in progress and on completed research findings undertaken through the DCN
facilitatesgreater public acceptance where necessary for any research undertaken
We believe that there are three key principles central to carrying out research ethically:
Obtaining informed consent - DCN members need to be able to make an informed decision about whether or not to take part in research. To be able to do this, they will need to know and understand the purpose of the research and what it involves.
Protecting participants from harm - Both those taking part in the research and doing the research should be safeguarded from harm (both physical and psychological).
Maintaining confidentiality and anonymity - The confidentiality and anonymity of participants should be protected when storing and handling data.
What does this policy mean for DCN members asked to take part in research?
The DCN has developed a checklist to try to ensure that research involving the DCN is conducted appropriately and is relevant to our members. Although it is not possible to cover all potential issues, the research checklist has been developed to highlight some that might arise. Hopefully DCN members will feel confident that any research they are asked to take part in is a good and necessary piece of work and will help towards understanding the various issues associated with donor conception. The research should be explained to DCN members clearly, and once the study is finished they should be told about the results.
If DCN members have been asked to take part in a research project and have any questions about it, they should contact the researcher.
What does this policy mean for researchers wanting to conduct a research project?
If a research project involves collecting information from or about members of the DCN researchers must complete the checklist.
If the proposed research has been approved by a Research Ethics Committee such as an NHS institution or University, please send a copy of the approval and supporting documents.
In addition to Research Ethics Committee approval, the proposal will still require operational approval from the DCN Research Group. A proposal can be approved, amendments suggested or further information required. In some cases a proposal can be rejected.
It is the researcher’s responsibility to ensure that the research is carried out in accordance with approval from the appropriate Research Ethics Committee.
Once the research has taken place the researcher must ensure that there is easy access to the findings when they are published e.g. the researcher is encouraged to write a piece for the newsletter or present them at a DCN meeting. Summaries of findings and publicaitons will be placed on our website.
What does this policy mean for the DCN?
Before the research takes place, the DCN is responsible for ensuring that the research group has reviewed the checklist and submitted research documentation and that a response is provided to the researcher within 30 days. As stated above, this can be approval for the research to take place under the auspices of the DCN, a request for amendments or further information or a rejection. The DCN is NOT responsible for carrying out the research, nor ensuring that it follows the approval of the Research Ethics Committee, or for any implications of its findings. This is the sole responsibility of the researcher.