An online survey exploring the experiences of women with ADHD
Diagnosis and Experiences from Women with ADHD; an International Survey
This study is trying to learn about the experiences of women with ADHD by asking them to share their thoughts on symptoms, treatment, and the challenges they face.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 3000 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Parnassia Groep Academic / other |
| Locations | 1 site (Den Haag) |
| Trial ID | NCT06169709 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather insights from women with ADHD through a cross-sectional online survey. It focuses on understanding their experiences related to ADHD symptoms, diagnosis, treatment, and support, as well as identifying barriers they face. The study will also assess how ADHD affects various life domains and calculate the prevalence of associated health conditions. Ultimately, it seeks to highlight areas for future research that are important to women with ADHD.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18 and older who have ADHD, whether diagnosed by a healthcare professional or self-diagnosed.
Not a fit: Patients who are unable to read, understand, or sign the informed consent form will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of ADHD in women, leading to improved treatment and support strategies.
How similar studies have performed: While there is ongoing research into ADHD, this specific focus on women's experiences is relatively novel and underexplored.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Identify as a woman * Aged 18 or above * Have ADHD (both diagnosed by a health professional and self-diagnosed) Exclusion Criteria: * People who are not able to read, understand, or sign the information letter or informed consent form are excluded from participation.
Where this trial is running
Den Haag
- Parnassia Groep — Den Haag, Netherlands (Recruiting)
Study contacts
- Principal investigator: Sandra Kooij, Prof. dr. — PsyQ
- Study coordinator: Daniëlle de Graaf-Starreveld, PhD
- Email: femaleadhd@psyq.nl
- Phone: +31 88 35 711 93
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.