The Focus is to Investigate Effect of an Educational Video on Fecundity Knowledge Among Young AdultsNCT06631950
Young Adults' Fecundity Knowledge and Fertility Intentions and Reproductive Behavior
A study testing Educational intervention in people with The Focus is to Investigate Effect of an Educational Video on Fecundity Knowledge Among Young Adults, run by University of Aarhus at 2 sites in 2 countries.
Trial summary
This RCT investigates the impact of an educational video on fecundity knowledge among young adults. The video discusses several risk factors associated with fecundity, such as age and smoking. The primary outcome measure of the RCT is fecundity knowledge. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- The Focus is to Investigate Effect of an Educational Video on Fecundity Knowledge Among Young Adults
- What is being tested?
- Educational intervention
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10,000 participants
- Where
- 2 sitesin 2 countries
- Study dates
- 26 Nov 2024to Oct 2045
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Offspring of mothers part of the DNBC and MoBa cohorts
- Being of legal age
- Responded to the Global Questionnaire at baseline
Who cannot join
- Being underage
- Not understanding Norwegian/Danish language
Trial locations and contacts
2 sites in 2 countries. Contact the study team or a site near you to ask about taking part.
2 sites in 2 countries
Denmark1 site, 1 recruiting
- Recruiting
Aarhus University/DNBC/SSI
Aarhus
Gritt Marie Hviid Malling, +45 29660956, gritt.malling@sund.ku.dk
Cecilia Ramlau-Hansen, Professor
About this study
Official title: A Video Intervention on Young Adults' Fertility Awareness: a Large-scale Educational RCT in Denmark and Norway Measuring Fecundity Knowledge, Fertility Intentions, Reproductive Behavior and Long-run Impacts on Realized Fertility
This RCT investigates the impact of an educational video on fecundity knowledge among young adults. The video discusses several risk factors associated with fecundity, such as age and smoking. The primary outcome measure of the RCT is fecundity knowledge. The knowledge level is defined based on the following factors: Age; smoking; sexually transmitted infections; Success of spontaneous pregnancy according to female age; Success of pregnancy according to female age and fertility treatment. The secondary outcomes are: intentions regarding the timing of desired pregnancy/childbirth; fecundity-protective behaviors; life goals; realized fertility later in life.
Read the detailed description
This study is an experimental randomized controlled trial (RCT) based on data from the Danish National Birth Cohort (DNBC) and the Norwegian Mother and Child Cohort Study (MoBa). The RCT consists of young adult offspring from these two birth cohorts. The participants in the subsample will randomly be assigned to either an intervention or a control group. The RCT is part of the research project BIOSFER which is funded by an ERC Synergy Grant (European Union, 101071773). The research project aims to investigate the biologic and social causes of low fertility in modern societies.
The Danish National Birth Cohort (DNBC) is an ongoing nationwide cohort of women and their children with more than 20 years of follow-up data (Olsen et al., 2001). The cohort contains 92,000 women recruited 1996 to 2002, who experienced 100,000 pregnancies in total. It has a rich set of background variables including child's development and health up to 18 years, as well as self-reported measures from age 18 onwards. The oldest offspring in the DNBC will be 29 years old at the time of treatment.
The Norwegian Mother, Father and Child Cohort Study (MoBa) is built around 110,000 pregnancies recruited between 1999 and 2008 (Magnus et al., 2016). Children have reported on their own health and exposures from the age of 13, and health and socioeconomic status were reported by the parents before this age. The RCT study will be conducted on a subsample of the MoBa children who are at least 18 years old as of 2024. The oldest offspring in the MoBa will be 25 years old at the time of treatment.
Data collection for the RCT will take place between late 2024 and mid-2025. The RCT intervention group will receive a fecundity knowledge intervention. The intervention consists of a short (3 minutes) animated educational video containing information on risk factors of importance for fecundity.
The primary outcome measure of the RCT is fecundity knowledge. The knowledge level is defined based on the following factors: Age; smoking; sexually transmitted infections; Success of spontaneous pregnancy according to female age; Success of pregnancy according to female age and fertility treatment. The secondary outcomes are: intentions regarding the timing of desired pregnancy/childbirth; fecundity-protective behaviors; life goals; future reproductive behavior- including attempts to conceive, termination of pregnancies and realized fertility The primary and secondary outcomes are measured with validated self-reported questionnaire items - except for certain items under reproductive behavior, such as 'realized fertility', which is measured through registries.
The target group is adult offspring of the two cohorts, the DNBC and MoBa. Outcomes of the trial will be analyzed for the total population participating in the RCT; for specific age-groups; for men and women; by socioeconomic status of the individuals and their families or origin; and for individuals with high and low risk preferences (measured through questionnaires).
Hypothesis: young adult women and men have low-moderate fecundity knowledge and an educational digital intervention will have an impact on the interventions' group fecundity knowledge and influence a) their family building intentions to desire a first and/or last child at a younger age, b) their fecundity-protective behaviors, c) their priority of life goals, d) their future reproductive behavior, including attempts to conceive, termination of pregnancies and realized fertility.
The goal is to enhance young adults' fecundity knowledge in order to secure that adults are able to make well-informed decisions regarding their family building and reproductive choices.
Individuals who are included in the RCT sample, will be randomized 1:1 by simple randomization to one of the following study arms:
- Experimental arm (fecundity knowledge intervention group). In the experimental arm, Individuals receive a short (3 minutes) animated educational video on risk factors of importance for fecundity.
II. Control arm (no fecundity knowledge provided).
The investigators will use computer-based randomization methods. When analyzing the data, the data set will by necessity contain information on whether each individual is in the intervention or control group. Coding and classification of outcome variables will be done jointly for the intervention and control group, so this knowledge will not influence the investigators handling of the data.
The intervention group will be provided with information that should allow them to correctly answer questions on fecundity knowledge and fecundity risks factors. The fecundity information will be provided through a short animated educational video that will be sent out digitally. The control group is not receiving such information. As part of the overall BIOSFER project, all offspring in both birth cohorts have received a Global Questionnaire at baseline including items and scales measuring fecundity knowledge and the participants' family formation/intentions regarding family formation and views on life goals. Only participants' having responded to the Global Questionnaire will be invited to the RCT study. After the intervention, both the intervention and the control group will receive identical questionnaire items and scales on fecundity knowledge and intentions regarding family formation, and their views on life goals. Hence, all the respondents receive the questions that inform our outcome variables both before and after the intervention. The participants in the intervention and control group will also be asked about their fecundity-protective behavior.
Statistical analysis and interpretation of data:
Overall, 13,106 (23%) of MoBa participants have responded to the Global Questionnaire. In DNBC data collection of the Global Questionnaire will continue until April 2025. Currently, 11,900 (27% of those who has been invited so far) have responded to the Global Questionnaire. Participants responding to the Global Questionnaire in DNBC and MoBa will receive an invitation to the RCT study.
For the sample size calculation for the primary outcome the investigators expect a participation of 30%. This is based on previous response rates within similar data collections in the two cohorts. Power calculations for the primary outcome were performed with a 5% significance level. The investigators follow convention and use 80% power as a cutoff for sufficient power. Assuming a response rate of 30, there will be power to detect effects down to 5 percent (2.5pp) in the full sample, and 10 percent (5 pp) among women and men when analyzed separately.
The investigators also performed power calculations assessing how power varies as a function of sample size and effect size. The MoBa cohort is used as example, where the RCT invitation will be sent to all 13 106 respondents of the MoBa Global Questionnaire. The investigators also assess the power for sex-specific analysis, with 8325 women and 4723 men (58 answering "other" are excluded from these). The power calculation assumes an even split between groups, and then tests the power for difference in means.
In the power calculations, the investigators use a "fertility knowledge percentage correct score" (see e.g. Bunting et al 2013), with a range from 0 to 100%. The investigators assume a baseline of knowledge of 50 percentage points, somewhat less than what was found in Bunting et al. 2013 (65-68 points). The investigators expect the knowledge level to be lower in our population compared to the population in Bunting et al. 2013. The population in this study is younger (18-29) compared to Bunting et al.'s (31.8 years old). Further, 26% of Bunting et al.'s population already had children, which is expected to be lower in our population. Hence, younger age and not being a parent will most likely effect the knowledge level. With a standard deviation of 25 (taken from Bunting et al. 2013 p. 389), the investigators then assess the power to detect effects of 2.5, 5, 7.5 and 10 percentage points.
Across all samples and down to a 10% response rate, the investigators can detect effects of 7.5 percentage points or higher. In the combined sample, the investigators can detect effects as small as 5 percentage points at a 10% response rate. To detect the smallest effects (2.5 percentage points), a 30% response rate is required for the combined sample.
For women, the investigators can detect effects as small as 5 percentage points with a 10% response rate. To detect effects of 2.5 percentage points require a 40% response rate. In the male sample, effects of 7.5 percentage points and larger can be detected with a 10% response rate. Detecting a 5 pp effect requires 20% response, and 2.5 pp requires more than 50% response.
The effectiveness of the RCT will be analyzed using an intention-to-treat (ITT) approach.
The results of the quantitative evaluation (primary and secondary outcomes) is planned to be analyzed and published in more than one scientific paper.
The quantitative evaluation of RCT is complemented by a qualitative evaluation looking into the participants' thoughts on the fecundity knowledge intervention, highlighting what works for whom under which circumstances, but also their overall thought on family formation.
- Conditions
- The Focus is to Investigate Effect of an Educational Video on Fecundity Knowledge Among Young Adults
- Being tested
- Educational intervention
- Keywords
- Fecundity knowledge, Fertility awareness, Family intentions, Video intervention
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Educational interventionOther
The educational intervention group will be provided with information that should allow them to correctly answer questions on fecundity knowledge and fecundity risks factors. The fecundity information will be provided through a short animated educational video (3 minutes) that will be sent out digitally. The control group is not receiving such information.
| Study group | Role | What they receive |
|---|---|---|
| Fecundity knowledge intervention | Experimental | In the experimental arm, participants receive a short (3 minutes) educational video on risk factors of importance for fecundity. Receives: Other: Educational intervention |
| Control | No intervention | In the no-intervention arm, the participants do not receive the intervention (a short educational video). |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in fecundity knowledge
Fecundity knowledge level in intervention arm versus control arm. Fecundity knowledge is measured with validated self-reported questionnaire items; revised Cardiff Fertility Knowledge Scale. The values range from 1-100, higher scores indicate higher knowledge level.
The knowledge level is defined as change in knowledge level of the following factors:
- Age, smoking, STI (Chlamydia)
- Success of spontaneous pregnancy according to female age
- Success of pregnancy according to female age and fertility treatment
Measured: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Secondary outcomes (7)
Change in intentions regarding timing of pregnancy/childbirth
Preferred age at first and last child in intervention group compared to the control group. Measured with self-reported questionnaire items.
Probability of intending to have a child in the near future (1-2 years), and in the relatively near future (up to 4-5 years)
Measured: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Change in life goals
Life goals in the intervention group, compared to the control group, are shifted toward emphasis on childbearing and union formation relative to other life goals. Measured with self-reported questionnaire items.
Measured: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Change in adopting fecundity-protective behaviors
Intentions of adoption fecundity-protective behaviors in the intervention group compared to the control group. Measured with self-reported questionnaire items.
Measured: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Change in realized fertility (followed up in registers)
Total number of children in the intervention group compared to the control group. Followed up in national birth registers' after the intervention.
Measured: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Change in realized fertility (followed up in registers)
Mean age at first and at last child in the intervention group compared to the control group. Followed up in national birth registers' after the intervention.
Measured: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Change in realized fertility (followed up in registers)
Total number of pregnancy terminations in the intervention group compared to the control group. Followed up in national birth registers' after the intervention.
Measured: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Change in realized fertility (followed up in registers)
Mean age at first and at last pregnancy termination in the intervention group compared to the control group. Followed up in national birth registers' after the intervention.
Measured: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Oct 2024
- Study start26 Nov 2024
- Primary completionDec 2025 (estimated)
- Study completionOct 2045 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for The Focus is to Investigate Effect of an Educational Video on Fecundity Knowledge Among Young AdultsStudies of the same condition, open and under way.
- More trials run by University of AarhusThe 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
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 10,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Aarhus
- Sponsor type
- University, hospital or other
- Collaborators
- Danish National Birth Cohort (DNBC), Norwegian Mother and Child Cohort Study (MoBa), European Union
- Responsible party
- Sponsor
- Investigators
- Mikko Myrskylä, Professor, Principal investigator, Max Planck Institute for Demographic Research, Rostock, GermanyCecilia Ramlau-Hansen, Professor, Principal investigator, Department of Public Health - Department of Epidemiology, Aarhus University, DenmarkSiri Eldevik Håberg, Professor, Principal investigator, Centre for Fertility and Health, Norwegian Institute of Public Health, Norway
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06631950
- Sponsor's protocol ID
- BIOSFER RCT - 101071773
- Status last verified
- Mar 2025
- First submitted
- 20 Sep 2024
- Last updated
- 2 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: For data access, parties must contact DNBC and/or MoBa directly. The new research project must be approved by Danish or/and the Norwegian authorities and follow the procedures for data access in the DNBC/MoBa. All costs for assessing data will be covered by the party requesting the data.
Study at a glance
From the registry record, last updated by the sponsor on 2 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Video Intervention on Young Adults' Fertility Awareness: a Large-scale Educational RCT in Denmark and Norway Measuring Fecundity Knowledge, Fertility Intentions, Reproductive Behavior and Long-run Impacts on Realized Fertility
- ClinicalTrials.gov ID
- NCT06631950
- Acronym / sponsor ID
- BIOSFER RCT - 101071773
- Conditions
- The Focus is to Investigate Effect of an Educational Video on Fecundity Knowledge Among Young Adults
- Keywords
- Fecundity knowledge, Fertility awareness, Family intentions, Video intervention
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 10,000 participants (estimated)
- Lead sponsor
- University of AarhusUniversity, hospital or other
- Collaborators
- Danish National Birth Cohort (DNBC), Norwegian Mother and Child Cohort Study (MoBa), European Union
- Study start
- 26 Nov 2024 (actual)
- Primary completion
- Dec 2025 (estimated)
- Study completion
- Oct 2045 (estimated)
- First posted
- 8 Oct 2024 (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.
This RCT investigates the impact of an educational video on fecundity knowledge among young adults. The video discusses several risk factors associated with fecundity, such as age and smoking. The primary outcome measure of the RCT is fecundity knowledge. The knowledge level is defined based on the following factors: Age; smoking; sexually transmitted infections; Success of spontaneous pregnancy according to female age; Success of pregnancy according to female age and fertility treatment. The secondary outcomes are: intentions regarding the timing of desired pregnancy/childbirth; fecundity-protective behaviors; life goals; realized fertility later in life.
Detailed description
This study is an experimental randomized controlled trial (RCT) based on data from the Danish National Birth Cohort (DNBC) and the Norwegian Mother and Child Cohort Study (MoBa). The RCT consists of young adult offspring from these two birth cohorts. The participants in the subsample will randomly be assigned to either an intervention or a control group. The RCT is part of the research project BIOSFER which is funded by an ERC Synergy Grant (European Union, 101071773). The research project aims to investigate the biologic and social causes of low fertility in modern societies.
The Danish National Birth Cohort (DNBC) is an ongoing nationwide cohort of women and their children with more than 20 years of follow-up data (Olsen et al., 2001). The cohort contains 92,000 women recruited 1996 to 2002, who experienced 100,000 pregnancies in total. It has a rich set of background variables including child's development and health up to 18 years, as well as self-reported measures from age 18 onwards. The oldest offspring in the DNBC will be 29 years old at the time of treatment.
The Norwegian Mother, Father and Child Cohort Study (MoBa) is built around 110,000 pregnancies recruited between 1999 and 2008 (Magnus et al., 2016). Children have reported on their own health and exposures from the age of 13, and health and socioeconomic status were reported by the parents before this age. The RCT study will be conducted on a subsample of the MoBa children who are at least 18 years old as of 2024. The oldest offspring in the MoBa will be 25 years old at the time of treatment.
Data collection for the RCT will take place between late 2024 and mid-2025. The RCT intervention group will receive a fecundity knowledge intervention. The intervention consists of a short (3 minutes) animated educational video containing information on risk factors of importance for fecundity.
The primary outcome measure of the RCT is fecundity knowledge. The knowledge level is defined based on the following factors: Age; smoking; sexually transmitted infections; Success of spontaneous pregnancy according to female age; Success of pregnancy according to female age and fertility treatment. The secondary outcomes are: intentions regarding the timing of desired pregnancy/childbirth; fecundity-protective behaviors; life goals; future reproductive behavior- including attempts to conceive, termination of pregnancies and realized fertility The primary and secondary outcomes are measured with validated self-reported questionnaire items - except for certain items under reproductive behavior, such as 'realized fertility', which is measured through registries.
The target group is adult offspring of the two cohorts, the DNBC and MoBa. Outcomes of the trial will be analyzed for the total population participating in the RCT; for specific age-groups; for men and women; by socioeconomic status of the individuals and their families or origin; and for individuals with high and low risk preferences (measured through questionnaires).
Hypothesis: young adult women and men have low-moderate fecundity knowledge and an educational digital intervention will have an impact on the interventions' group fecundity knowledge and influence a) their family building intentions to desire a first and/or last child at a younger age, b) their fecundity-protective behaviors, c) their priority of life goals, d) their future reproductive behavior, including attempts to conceive, termination of pregnancies and realized fertility.
The goal is to enhance young adults' fecundity knowledge in order to secure that adults are able to make well-informed decisions regarding their family building and reproductive choices.
Individuals who are included in the RCT sample, will be randomized 1:1 by simple randomization to one of the following study arms:
- Experimental arm (fecundity knowledge intervention group). In the experimental arm, Individuals receive a short (3 minutes) animated educational video on risk factors of importance for fecundity.
II. Control arm (no fecundity knowledge provided).
The investigators will use computer-based randomization methods. When analyzing the data, the data set will by necessity contain information on whether each individual is in the intervention or control group. Coding and classification of outcome variables will be done jointly for the intervention and control group, so this knowledge will not influence the investigators handling of the data.
The intervention group will be provided with information that should allow them to correctly answer questions on fecundity knowledge and fecundity risks factors. The fecundity information will be provided through a short animated educational video that will be sent out digitally. The control group is not receiving such information. As part of the overall BIOSFER project, all offspring in both birth cohorts have received a Global Questionnaire at baseline including items and scales measuring fecundity knowledge and the participants' family formation/intentions regarding family formation and views on life goals. Only participants' having responded to the Global Questionnaire will be invited to the RCT study. After the intervention, both the intervention and the control group will receive identical questionnaire items and scales on fecundity knowledge and intentions regarding family formation, and their views on life goals. Hence, all the respondents receive the questions that inform our outcome variables both before and after the intervention. The participants in the intervention and control group will also be asked about their fecundity-protective behavior.
Statistical analysis and interpretation of data:
Overall, 13,106 (23%) of MoBa participants have responded to the Global Questionnaire. In DNBC data collection of the Global Questionnaire will continue until April 2025. Currently, 11,900 (27% of those who has been invited so far) have responded to the Global Questionnaire. Participants responding to the Global Questionnaire in DNBC and MoBa will receive an invitation to the RCT study.
For the sample size calculation for the primary outcome the investigators expect a participation of 30%. This is based on previous response rates within similar data collections in the two cohorts. Power calculations for the primary outcome were performed with a 5% significance level. The investigators follow convention and use 80% power as a cutoff for sufficient power. Assuming a response rate of 30, there will be power to detect effects down to 5 percent (2.5pp) in the full sample, and 10 percent (5 pp) among women and men when analyzed separately.
The investigators also performed power calculations assessing how power varies as a function of sample size and effect size. The MoBa cohort is used as example, where the RCT invitation will be sent to all 13 106 respondents of the MoBa Global Questionnaire. The investigators also assess the power for sex-specific analysis, with 8325 women and 4723 men (58 answering "other" are excluded from these). The power calculation assumes an even split between groups, and then tests the power for difference in means.
In the power calculations, the investigators use a "fertility knowledge percentage correct score" (see e.g. Bunting et al 2013), with a range from 0 to 100%. The investigators assume a baseline of knowledge of 50 percentage points, somewhat less than what was found in Bunting et al. 2013 (65-68 points). The investigators expect the knowledge level to be lower in our population compared to the population in Bunting et al. 2013. The population in this study is younger (18-29) compared to Bunting et al.'s (31.8 years old). Further, 26% of Bunting et al.'s population already had children, which is expected to be lower in our population. Hence, younger age and not being a parent will most likely effect the knowledge level. With a standard deviation of 25 (taken from Bunting et al. 2013 p. 389), the investigators then assess the power to detect effects of 2.5, 5, 7.5 and 10 percentage points.
Across all samples and down to a 10% response rate, the investigators can detect effects of 7.5 percentage points or higher. In the combined sample, the investigators can detect effects as small as 5 percentage points at a 10% response rate. To detect the smallest effects (2.5 percentage points), a 30% response rate is required for the combined sample.
For women, the investigators can detect effects as small as 5 percentage points with a 10% response rate. To detect effects of 2.5 percentage points require a 40% response rate. In the male sample, effects of 7.5 percentage points and larger can be detected with a 10% response rate. Detecting a 5 pp effect requires 20% response, and 2.5 pp requires more than 50% response.
The effectiveness of the RCT will be analyzed using an intention-to-treat (ITT) approach.
The results of the quantitative evaluation (primary and secondary outcomes) is planned to be analyzed and published in more than one scientific paper.
The quantitative evaluation of RCT is complemented by a qualitative evaluation looking into the participants' thoughts on the fecundity knowledge intervention, highlighting what works for whom under which circumstances, but also their overall thought on family formation.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Fecundity knowledge intervention | Experimental | Other: Educational interventionIn the experimental arm, participants receive a short (3 minutes) educational video on risk factors of importance for fecundity. |
| Control | No intervention | –In the no-intervention arm, the participants do not receive the intervention (a short educational video). |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Offspring of mothers part of the DNBC and MoBa cohorts
- Being of legal age
- Responded to the Global Questionnaire at baseline
Key exclusion criteria (2 listed)
- Being underage
- Not understanding Norwegian/Danish language
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 |
|---|---|---|
| Educational interventionThe educational intervention group will be provided with information that should allow them to correctly answer questions on fecundity knowledge and fecundity risks factors. The fecundity information will be provided through a short animated educational video (3 minutes) that will be sent out digitally. The control group is not receiving such information. | Other | Fecundity knowledge intervention |
Primary outcome
Change in fecundity knowledge
Time frame: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Fecundity knowledge level in intervention arm versus control arm. Fecundity knowledge is measured with validated self-reported questionnaire items; revised Cardiff Fertility Knowledge Scale. The values range from 1-100, higher scores indicate higher knowledge level. The knowledge level is defined as change in knowledge level of the following factors: * Age, smoking, STI (Chlamydia) * Success of spontaneous pregnancy according to female age * Success of pregnancy according to female age and fertility treatment
7 secondary outcomes
Change in intentions regarding timing of pregnancy/childbirth
Time frame: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Change in life goals
Time frame: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Change in adopting fecundity-protective behaviors
Time frame: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts
Change in realized fertility (followed up in registers)
Time frame: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Change in realized fertility (followed up in registers)
Time frame: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Change in realized fertility (followed up in registers)
Time frame: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Change in realized fertility (followed up in registers)
Time frame: 3, 5, 10 years and 20 years follow-up in national birth registers' after the intervention.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Apr 2025.
- Individual participant dataSharing planned: Yes. For data access, parties must contact DNBC and/or MoBa directly. The new research project must be approved by Danish or/and the Norwegian authorities and follow the procedures for data access in the DNBC/MoBa. All costs for assessing data will be covered by the party requesting the data.
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.
Mikko Myrskylä, Professor principal investigator
Max Planck Institute for Demographic Research, Rostock, Germany
Cecilia Ramlau-Hansen, Professor principal investigator
Department of Public Health - Department of Epidemiology, Aarhus University, Denmark
Siri Eldevik Håberg, Professor principal investigator
Centre for Fertility and Health, Norwegian Institute of Public Health, Norway
2 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Educational intervention in people with The Focus is to Investigate Effect of an Educational Video on Fecundity Knowledge Among Young Adults, run by University of Aarhus at 2 sites in 2 countries.
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 2 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: looking for participants now, as of the sponsor's last update on 2 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Denmark, Norway. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Gritt Marie Hviid Malling, PhD student (+4529660956, gritt.malling@sund.ku.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in fecundity knowledge (time frame: Measured immediately after intervention (educational video), and at a later point of time (likely within 1-2 years) depending on the data collection logistics for the two cohorts). 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 2 Apr 2025.