Sleep, Oxytocin and Reward Processing in Women in the Postpartum Phase
This study is not yet recruiting. It focuses on depression and currently lists study information in Sweden.
Key information made simple
This study is looking at explore the relationship between sleep, oxytocin, and reward processing in new mothers for people with Postpartum Depression. Participants mainly provide questionnaire, assessment, or follow-up information rather than receiving a new study treatment. Taking part may give some people access to a digital support tool with regular follow-up, but direct benefit is not guaranteed.
Your next step
The official record suggests a mix of remote and in-person participation through a university, with sites including University of Uppsala. Participation appears to center on assessments, scans, or samples rather than trying a new treatment. The main fit is usually being able to understand the study and consent and meeting the main study requirements, while common reasons not to take part include other factors that could make participation unsuitable. The official record does not list a trial phase, which usually means the study is focused on observation rather than testing a staged treatment.
Questions to ask before joining
- What are the exact eligibility criteria, and what could exclude someone?
- How many visits, assessments, or follow-ups are expected, and over what period?
- What risks, side effects, practical burdens, or alternatives should be understood first?
- Who should be contacted to confirm locations, timing, compensation, and next steps?
Things to check before joining
- Recruitment status
- Not Yet Recruiting
- Estimated enrollment
- Not clearly listed
- Sponsor
- International Research Training Group 2804
- Sponsor type
- Unknown or unclear
- Study type
- Other
- Intervention type
- Device / app / digital / technology
- Study phase
- Not clearly listed
- Locations
- Sweden
- Age range
- Over 18 Years
- Official registry ID
- NCT06711809
- Official source
- Official registry link
Want help reviewing this study?
Key study information
- Condition
- Depression
- Study status
- Not Yet Recruiting
- Sponsor / lead affiliation
- International Research Training Group 2804
- Location / country
- Sweden
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT06711809
Why this study may matter
This study may matter because it adds public evidence around depression. HopeStage presents it as a starting point for understanding the study, checking the official source, and preparing questions with a care team.
For you
Taking part may help clarify how this condition is measured or understood.
It requires regular follow-up, often through questionnaires or interviews.
Mixes in-person and remote participation.
Registry reference
This page links back to the public source record so people can verify details directly with the registry and research team.
If you want the full study description, eligibility criteria, locations, and sponsor information in the original format, this is the place to check before taking the next step.
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT06711809
Not medical advice
Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com
Questions about this study
What is this study trying to understand?
This study is exploring digital app or tool for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.
Does this study involve a device, app, or technology?
This appears to be a device / app / digital / technology study. The phase is not clearly listed in the public registry. Phase is mostly relevant for medication studies and some device studies. For this study, it may be more useful to look at what is required, the duration, visits, and eligibility criteria.
Who might this study be for?
This study may concern people with depression; age range: Over 18 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may need to use a device, app, or digital tool for a defined period. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
What should I check about data, monitoring, alerts, and daily use?
If the study uses a device, app, or digital tool, check what data is collected, who can access it, how often you need to use it, and what happens if the tool detects a concerning signal. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by International Research Training Group 2804, which appears to be unknown or unclear. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The registry indicates that this study has not started recruiting yet. You can check the planned start date and available contacts.
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