Reproductive HealthNCT07601581
A Trial to Determine People's Explicit vs. Implicit Preferences for Gender-inclusive Sexual and Reproductive Health Content
A study testing Read reproductive health material and review in people with Reproductive Health, run by Boston Children's Hospital at 1 site in United States.
Trial summary
Participants will be shown two different versions of health content and asked which they prefer. Read more about this study
- Who is it for?
- Ages 18 to 64 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Reproductive Health
- What is being tested?
- Read reproductive health material and review
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 454 participants
- Where
- 1 siteUnited States
- Study dates
- 30 Dec 2024to 1 Mar 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 64 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Female sex assigned at birth
- Can read and write in English
- Reproductive age adults (18-64)
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
United States1 site
Boston Children's Hospital
Boston, Massachusetts, 02115
About this study
Official title: A Randomized, Controlled Trial to Determine People's Explicit vs. Implicit Preferences for Gender-inclusive Sexual and Reproductive Health Content
Participants will be shown two different versions of health content and asked which they prefer.
- Conditions
- Reproductive Health
- Being tested
- Read reproductive health material and review
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Read reproductive health material and reviewBehavioural
Participants will read reproductive health information and review.
| Study group | Role | What they receive |
|---|---|---|
| Gender Specific | Experimental | Not described Receives: Behavioral: Read reproductive health material and review |
| Gender Inclusive | Experimental | Not described Receives: Behavioral: Read reproductive health material and review |
What is being measured
The primary outcome is the main question the study is designed to answer.
Content Review
For each piece of content, participants will rate the following questions on a scale from strongly agree to strongly disagree: 1) I found this content easy to understand, 2) I found this content to be reliable, 3) I found this content to be biased, 4) This content is meant for people like me, 5) This content is relevant to people like me. Higher scores mean the person agreed with more positive statements.
Measured: Baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 May 2026
- Study start30 Dec 2024
- Primary completion5 Jan 2025
- Study completion1 Mar 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Reproductive HealthStudies of the same condition, open and under way.
- More trials run by Boston Children's HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Enrolment
- 454 participants (actual)
Sponsor and investigators
- Lead sponsor
- Boston Children's Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- GLMA: Health Professionals Advancing LGBTQ+ Equality
- Responsible party
- Principal investigator, Elizabeth Boskey, Boston Children's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07601581
- Sponsor's protocol ID
- IRB-P00047950
- Status last verified
- May 2026
- First submitted
- 12 May 2026
- Last updated
- 22 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The datasets generated or analyzed during this study are available from the corresponding author on reasonable request, with the completion of a signed data use agreement.
Study at a glance
From the registry record, last updated by the sponsor on 22 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Controlled Trial to Determine People's Explicit vs. Implicit Preferences for Gender-inclusive Sexual and Reproductive Health Content
- ClinicalTrials.gov ID
- NCT07601581
- Acronym / sponsor ID
- IRB-P00047950
- Conditions
- Reproductive Health
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 454 participants (actual)
- Lead sponsor
- Boston Children's HospitalUniversity, hospital or other
- Collaborators
- GLMA: Health Professionals Advancing LGBTQ+ Equality
- Study start
- 30 Dec 2024 (actual)
- Primary completion
- 5 Jan 2025 (actual)
- Study completion
- 1 Mar 2025 (actual)
- First posted
- 22 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Participants will be shown two different versions of health content and asked which they prefer.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Gender Specific | Experimental | Behavioral: Read reproductive health material and review |
| Gender Inclusive | Experimental | Behavioral: Read reproductive health material and review |
Who may qualify
- Ages
- 18 to 64 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Female sex assigned at birth
- Can read and write in English
- Reproductive age adults (18-64)
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Read reproductive health material and reviewParticipants will read reproductive health information and review. | Behavioural | Gender Inclusive, Gender Specific |
Primary outcome
Content Review
Time frame: Baseline
For each piece of content, participants will rate the following questions on a scale from strongly agree to strongly disagree: 1) I found this content easy to understand, 2) I found this content to be reliable, 3) I found this content to be biased, 4) This content is meant for people like me, 5) This content is relevant to people like me. Higher scores mean the person agreed with more positive statements.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 May 2026.
- Individual participant dataSharing planned: Yes. The datasets generated or analyzed during this study are available from the corresponding author on reasonable request, with the completion of a signed data use agreement.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Read reproductive health material and review in people with Reproductive Health, run by Boston Children's Hospital at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Content Review (time frame: Baseline). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 May 2026.