N/A
N=75
Feasibility Trial of the TELL Tool Intervention
Fertility Issues · Disclosure · Parenting
Bottom Line
View on ClinicalTrials.gov: NCT04841967 ↗Enrolled (actual)
75
Serious AEs
0.0%
Results posted
Jan 2024
Primary outcome: Primary: Number of Participants Who Disclosed the Donor Conception to Their Children — 23; 16 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- TELL Tool Intervention (Behavioral); eBook Attention Control (Behavioral)
- Age
- Adult, Older Adult · 21+ yrs
- Sex
- All
- Sponsor
- University of Illinois at Chicago
- Primary completion
- Sep 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Who Disclosed the Donor Conception to Their Children |
23; 16 | — |
| SECONDARY Change in Disclosure Intention |
— | — |
| SECONDARY Change in Disclosure Competence |
— | — |
| SECONDARY Change in Disclosure Anxiety |
— | — |
Summary
A radical paradigm shift is taking place where technology, notably the explosion in easy accessible direct-to-consumer genetic testing (e.g., 23andMe) and a high consumer interest in genealogy (e.g., Ancestry.com), has hijacked gamete (eggs, sperm) and embryo donation recipient parents' control over whether to inform their children about their donor conception. Historically, the practice of gamete donation has been shrouded in secrecy, however, the skyrocketing use of direct-to-consumer genetic testing means that at any point in an adult life, an uninformed donor-conceived person can learn their DNA does not match their presumed ancestry of their parents and family members, putting into question their genetic relatedness to their parents and launching a spiraling sequence of negative health consequences and trauma. Furthermore, the lack of one's knowledge about actual genetic heritage in the age of precision medicine can be enormously detrimental to health and can result in medical maltreatment, including death. To address this serious problem and in accordance with International Patient Decision Aid Standards, we developed a digital, tailored, multicomponent Tool to Empower ParentaL TeLling and Talking (i.e., TELL Tool). The objective of this R34 study is to examine the feasibility, acceptability, and preliminary effects of the TELL Tool intervention in a pilot randomized-controlled feasibility trial with 60 donor-recipient parents and 10 clinicians to determine intervention viability and inform a larger, efficacy trial. An eBook with content about good parenting principles serves as the attention control.
Eligibility Criteria
Inclusion Criteria Parents:
- Reside in the United States or one of its recognized territories
- Conceived 1 or more children via gamete (egg/sperm) or embryo donation who are currently between the ages of 1 - 16 years of age
- Have not informed their child(ren) about their donor conception origins
- Are 21 years-of-age or older
- English speaking
Inclusion Criteria Clinicians:
- Active practice as a healthcare professional (e.g., nurse, physician, psychologist, social worker)
- Provide education and/or counseling to gamete (eggs, sperm) and/or embryo donation recipient parents about disclosure to their children in the United States or one of its recognized territories
- Able to provide feedback and insight about new tools to assist gamete (eggs, sperm) and/or embryo donation recipient parents with disclosure to their donor-conceived children
- Are 21 years-of-age or older
- English speaking
Exclusion Criteria Parents:
- Have already disclosed the donor conception to their donor-conceived child or children
- Reside outside of the United States or one of its recognized territories
Exclusion Criteria Clinicians:
- Not directly involved in providing education and/or counseling to gamete (eggs, sperm) and/or embryo donation recipient parents about disclosure to their children
- Are a member of the research team
Data sourced from ClinicalTrials.gov (NCT04841967). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.