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UnknownNCT06390540

Mobile-Based Exercise in Postpartum Period

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

Depression, Mother-Infant InteractionBehavioralFrom 18 Years to 45 Years
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Study ID: NCT06390540. We help you review the study, but cannot decide medical eligibility.
In plain English

Key information made simple

What is this study testing?

This study is testing whether a digital tool or app may be useful for adults experiencing depression.

What would participation involve?

Participants may use a digital tool or app, complete questionnaires or follow-up assessments, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group.

Who is it mainly for?

This study appears to be mainly for adults with depression.

What should you check before joining?

Ask about whether participation can be remote and what device access is needed, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.

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 guided sessions or support activities with check-ins on how they fit into daily life. The main fit is usually matching the main diagnosis and having access to the required digital tools, while common reasons not to take part include pregnancy or breastfeeding and other treatments that could interfere with the study. The official record does not list a formal phase, which usually means this is focused more on feasibility, delivery, or support than a standard numbered clinical-trial phase.

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateEstimated: May 1, 2024
Recruitment status
Unknown
Estimated enrollment
Not clearly listed
Sponsor
Ankara University
Sponsor type
University
Study type
Behavioral
Intervention type
Behavioral / psychological / psychosocial
Study phase
Not clearly listed
Locations
Not clearly listed
Age range
From 18 Years to 45 Years
Official registry ID
NCT06390540
Official title
Mobile-Based Exercise in Postpartum Period
Official source
Official registry link

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Study ID: NCT06390540. We help you review the study, but cannot decide medical eligibility.
In practice

For you

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

It requires regular follow-up, often through questionnaires or interviews.

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 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. It includes a comparison with a control group. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.

What is a behavioral study?

This appears to be a behavioral / psychological / psychosocial study. Phase is mainly useful to check for medication studies and some device studies.

Who might this study be for?

This study may concern people with depression; age range: From 18 Years to 45 Years. The criteria appear fairly specific, 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 take part in sessions or exercises related to habits, thoughts, emotions, or behaviors.

Could this study affect my mood, habits, motivation, or stress?

Behavioral studies can involve habits, emotions, motivation, stress, sleep, or ways of thinking. Ask whether the intervention could affect your mood or stress, and who to contact if you feel worse. 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.

What practical constraints should I expect?

The likely practical burden appears moderate. Things to check include multiple visits or assessments. Ask the study team about duration, visits, possible compensation, data access, and what happens if you want to stop.

Who is behind this study?

This study is sponsored by Ankara University, which appears to be a university. 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 recruitment status is not clearly listed. Check the official registry or contact the study team.

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