Preimplantation Genetic Testing for Aneuploidy Counseling

NCT ID: NCT06018454

Last Updated: 2024-12-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

213 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-20

Study Completion Date

2024-11-29

Brief Summary

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Purpose: To evaluate preimplantation genetic testing counseling interventions on patients undergoing in vitro fertilization treatment.

Preimplantation genetic testing for aneuploidy (PGT) allows patients undergoing in vitro fertilization (IVF) to screen embryos for genetic disorders. Preimplantation genetic testing for aneuploidy (PGT-A) is the testing most commonly ordered, and it screens for whole chromosome and large partial chromosome duplications or deletions. Currently, patient counseling varies based on the clinic, ranging from appointments to group seminars with a genetic counselor (GC), geneticist or reproductive endocrinology and infertility (REI) physicians for education regarding PGT. Patient knowledge regarding PGT has been varied with some studies indicating sufficient knowledge, while other studies have shown a potential lack of knowledge. One study indicated a third of patients had regret regarding their decision of whether or not to use PGT-A during IVF and another study indicated patients who choose to undergo PGT did so for reasons that were not evidence based. Additionally, educational materials have been illustrated to be inconsistent and with inappropriate literacy in regards to PGT counseling. One study has shown the potential of improvement with written intervention amongst providers and patients in regards to PGT related to a single genetic condition. The investigators hope to assess the efficacy of PGT-A educational and counseling interventions on patients undergoing IVF.

Detailed Description

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Procedures: Patients undergoing IVF for the first time will be randomized to one of three groups

1. Provider counseling (current standard care) with pre-test
2. Handout on PGT-A and provider counseling (current standard care + educational intervention) with pre-test
3. Handout on PGT-A, provider counseling and brief genetic counselor counseling (current standard of care + educational and counseling interventions) with pre-test

All patients will receive provider counseling(current standard of care) on PGT-A during their new IVF clinic visit. All groups will take a pre-test on PGT-A prior to receiving provider counseling and (if in an intervention group) prior to receiving handout or handout with brief counseling on PGT-A from a genetic counselor. At the end of their clinic visit, all participants will complete a post-test on PGT-A.

Two weeks after their clinic visit, all participants will receive a 2nd post-test on PGT-A and the SURE questionnaire to assess retained knowledge about PGT-A and decisional conflict about their choice to use PGT-A in their treatment cycle.

As there is not a validated knowledge survey for PGT-A, investigators have developed their own for pre- and post-tests. In order to validate the survey prior to using it in this study, investigators plan to enroll the first 100 participants in a pilot study to validate the instrument. The number needed for validation will depend on how much pilot participants scores vary between pre and post test. Participants in the pilot portion of the study will be asked to complete a pre-test on PGT-A, read the informational handout about PGT-A, and then complete a post test on PGT-A prior to their IVF appointment. Statisticians will analyze the pilot data as received, and will inform investigators when a sufficient number has been reached for survey validation. Once validated, the pilot arm of the study will be closed and will begin enrolling participants in the randomized trial portion described above.

Conditions

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Patient Education

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Patients randomized with computer generated block randomization of ratio 1:1:1 to randomize women to either 10 minute genetic counseling intervention with handout, handout, or no interventions. Randomization allocation will be performed prior to study initiation through the Institute for Clinical and Translational Science (ICTS) via REDCap software.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Provider counseling with pre-test

Counseling regarding PGT-A only with a provider(current standard of care), pre-test provided.

Group Type NO_INTERVENTION

No interventions assigned to this group

Handout on PGT-A and provider counseling with pre-test

Counseling regarding PGT-A with a provider and review of a handout(educational intervention), pre-test provided.

Group Type EXPERIMENTAL

Handout on PGT-A

Intervention Type OTHER

Educational handout on PGT-A

Handout on PGT-A, provider counseling and brief genetic counselor counseling with pre-test

Counseling regarding PGT-A only with a provider, review of a handout(educational intervention) and genetic counseling (counseling intervention), pre-test provided.

Group Type EXPERIMENTAL

Handout on PGT-A

Intervention Type OTHER

Educational handout on PGT-A

Handout on PGT-A and genetic counseling

Intervention Type OTHER

Handout on PGT-A and genetic counseling session with a genetic counselor on PGT-A

Interventions

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Handout on PGT-A

Educational handout on PGT-A

Intervention Type OTHER

Handout on PGT-A and genetic counseling

Handout on PGT-A and genetic counseling session with a genetic counselor on PGT-A

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients undergoing in vitro fertilization (IVF)

Exclusion Criteria

* Patients who have previously undergone IVF would be excluded.
* Patients who have previously discussed PGT with a genetic counselor would be excluded.
* Patients who do not speak English will be excluded.
* Patients who are employees of the clinic would be excluded.
* Patients who have an indication for PGT-M or PGT-SR would be excluded.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Eyup Hakan Duran

OTHER

Sponsor Role lead

Responsible Party

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Eyup Hakan Duran

Principal investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Prapti Singh, DO

Role: STUDY_DIRECTOR

University of Iowa

Locations

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University of Iowa

Iowa City, Iowa, United States

Site Status

Countries

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United States

References

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Gebhart MB, Hines RS, Penman A, Holland AC. How do patient perceived determinants influence the decision-making process to accept or decline preimplantation genetic screening? Fertil Steril. 2016 Jan;105(1):188-93. doi: 10.1016/j.fertnstert.2015.09.022. Epub 2015 Oct 24.

Reference Type BACKGROUND
PMID: 26474735 (View on PubMed)

Lee I, Alur-Gupta S, Gallop R, Dokras A. Utilization of preimplantation genetic testing for monogenic disorders. Fertil Steril. 2020 Oct;114(4):854-860. doi: 10.1016/j.fertnstert.2020.05.045.

Reference Type BACKGROUND
PMID: 33040985 (View on PubMed)

Kaing A, Rosen MP, Quinn MM. Perceptions, motivations and decision regret surrounding preimplantation genetic testing for aneuploidy. Hum Reprod. 2020 Sep 1;35(9):2047-2057. doi: 10.1093/humrep/deaa154.

Reference Type BACKGROUND
PMID: 32756971 (View on PubMed)

Quinn MM, Juarez-Hernandez F, Dunn M, Okamura RJ, Cedars MI, Rosen MP. Decision-making surrounding the use of preimplantation genetic testing for aneuploidy reveals misunderstanding regarding its benefit. J Assist Reprod Genet. 2018 Dec;35(12):2155-2159. doi: 10.1007/s10815-018-1337-8. Epub 2018 Oct 18.

Reference Type BACKGROUND
PMID: 30334131 (View on PubMed)

McGowan ML, Burant CJ, Moran R, Farrell R. Patient education and informed consent for preimplantation genetic diagnosis: health literacy for genetics and assisted reproductive technology. Genet Med. 2009 Sep;11(9):640-5. doi: 10.1097/GIM.0b013e3181ac6b52.

Reference Type BACKGROUND
PMID: 19652605 (View on PubMed)

Early ML, Kumar P, Marcell AV, Lawson C, Christianson M, Pecker LH. Literacy assessment of preimplantation genetic patient education materials exceed national reading levels. J Assist Reprod Genet. 2020 Aug;37(8):1913-1922. doi: 10.1007/s10815-020-01837-z. Epub 2020 May 29.

Reference Type BACKGROUND
PMID: 32472448 (View on PubMed)

Early ML, Strodel RJ, Lake IV, Ruddy JA, Saba JA, Singh SM, Lanzkron S, Mack JW, Meier ER, Christianson MS, Pecker LH. Acceptable, hopeful, and useful: development and mixed-method evaluation of an educational tool about reproductive options for people with sickle cell disease or trait. J Assist Reprod Genet. 2022 Jan;39(1):183-193. doi: 10.1007/s10815-021-02358-z. Epub 2021 Nov 22.

Reference Type BACKGROUND
PMID: 34806131 (View on PubMed)

Singh P, Summers KM, Chanouha N, Thoeny R, Zorn A, Van Voorhis BJ, Sparks AE, Eapen A, Faro EZ, Pawlak SA, Duran EH. A randomized controlled trial of counseling and educational methods on preimplantation genetic testing for aneuploidy for patients pursuing in vitro fertilization. Fertil Steril. 2025 Nov 15;124(5 Pt 2):964-973. doi: 10.1016/j.fertnstert.2025.06.010. Epub 2025 Jun 14.

Reference Type DERIVED
PMID: 40523553 (View on PubMed)

Other Identifiers

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202208644

Identifier Type: -

Identifier Source: org_study_id