UnknownNCT05400382

Mindfulness to Reduce Post-cesarean Pain and Prevent Postpartum Depression

This study has public registry information. It focuses on depression and currently lists study information in Global.

Depression, Pain, PostoperativeBehavioralFrom 18 Years to 45 Years

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Study reference: NCT05400382. HopeStage can help you review the study, but cannot decide medical eligibility.

In plain English

Key information made simple

This study is looking at test the effect of a mobile mindfulness-based intervention on reducing post-cesarean delivery pain and preventing postpartum depression for people with Depression, Unipolar or Pain, Postoperative. Participants take part in Mindfulness and complete follow-up assessments. Taking part may give some people access to Mindfulness, but direct benefit is not guaranteed.

What to expect

Your next step

The official record does not clearly spell out the visit format, but it appears to be coordinated directly by the research team. Participation appears to involve a study treatment together with follow-up visits and routine safety or progress checks. Common reasons not to take part include other factors that could make participation unsuitable. The official record does not list a formal phase, which usually means this is focused more on feasibility, delivery, or support than a standard drug-development stage.

Before joining

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?

Study clarity

Things to check before joining

Study start dateEstimated: July 1, 2023

Time commitment: long follow-up or multiple visits
Study phase: Not available
Enrollment: Not available
Recruitment status: Unknown
Sponsor: University of Illinois at Urbana-Champaign
Sponsor type: University
Main activity: digital app or tool
Intervention: Not available
Source: Official registry link

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Public study data

Key study information

Official title: Mindfulness to Reduce Post-cesarean Pain and Prevent Postpartum Depression
Condition: Depression, Pain, Postoperative
Study status: Unknown
Sponsor / lead affiliation: University of Illinois at Urbana-Champaign
Location / country: Global
Registry: ClinicalTrials.gov
External trial ID: NCT05400382

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.

In practice

For you

Taking part may help test a support approach in real life.

It requires regular visits and structured follow-up.

Official source

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.

Official title: Mindfulness to Reduce Post-cesarean Pain and Prevent Postpartum Depression
Source: ClinicalTrials.gov
Official registry link: Open official registry
External trial ID: NCT05400382

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

FAQ

Questions about this study

What is Mindfulness to Reduce Post-cesarean Pain and Prevent Postpartum Depression?

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.

Who is behind this study, and what type of sponsor is it?

This study is sponsored by University of Illinois at Urbana-Champaign. Based on the sponsor name or official registry information, it appears to be a university. You should verify the details in the official registry record.

What does participation involve, what phase is it, and what should I ask about safety?

This study may involve digital app or tool, study visits, and assessments. The time commitment is long follow-up or multiple visits. The study phase is not available in HopeStage data. Check the official source record to see whether a phase is listed. Enrollment is not available in HopeStage data. HopeStage cannot say whether a study is safe or right for you. Before joining, ask the research team about possible risks, time commitment, visits, side effects, compensation, safety monitoring, and whether participation may affect your current care.

Where can I verify the study details?

Use the official source record linked on this page to check the full study description, recruitment status, eligibility criteria, locations, sponsor information, phase, enrollment, contact details, and any listed risks or requirements.

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