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Depression

Neural Mechanisms of Family-Focused Treatment for Youth Depression

Recruiting · Boston, Charlestown, Massachusetts

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For your time and travel

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Most need no insurance or papers

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Interpreters available

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Your choice

Voluntary — you can stop anytime

What is this study?

The goal of this interventional study is to compare the baseline neural mechanisms and parenting in depressed and non-depressed children and to examine baseline neural mechanisms and parenting as predictors of Family-Focused Treatment for Childhood-Depression (FFT-CD) outcomes. The main questions it aims to answer are: * What are differences between depressed and non-depressed participants on baseline neural and parenting indicators?

It is , overseen by an independent and licensed medical staff.

Read the full clinical description

The goal of this interventional study is to compare the baseline neural mechanisms and parenting in depressed and non-depressed children and to examine baseline neural mechanisms and parenting as predictors of Family-Focused Treatment for Childhood-Depression (FFT-CD) outcomes. The main questions it aims to answer are: * What are differences between depressed and non-depressed participants on baseline neural and parenting indicators? * Do baseline neural and parenting indicators predict response to FFT-CD? * Does change in parenting and neural functioning mediate change in depression from baseline to follow-up? Participants will: * complete baseline clinical measures * complete neuroimaging tasks via Functional Magnetic Resonance Imaging (fMR) * undergo a 12-session course of FFT-CD * complete follow up evaluations and neuroimaging

Who this study is looking for

In plain language, from the study's own rules. The study team confirms the full details with you — this isn't a final yes or no.

✅ You may be able to join if…

  • Children ages 7 to 12
  • The child has a current DSM-5 diagnosis of MDD, Persistent DD, or DDNOS, OR the child does not meet criteria for any DSM-5 mental health diagnosis (checked using K-SADS-PL)
  • The child lives with a parent(s) or guardian who is willing to participate
  • Parent/guardian must not be currently pregnant and must be able to read and understand consent forms
  • The child can take part in MRI scans (no MRI contraindications) and can participate in English

🚫 You may not be able to join if…

  • The child has a condition that would interfere with participation, such as autism spectrum disorder, psychosis, active substance abuse/dependence, or OCD (as assessed on K-SADS-PL)
  • The child has intellectual disability (as assessed on K-SADS-PL)
  • The child has severe conduct disorder that threatens home stability (e.g., juvenile justice or children’s protective service involvement) (as assessed on K-SADS-PL)
  • Either the youth or primary caregiver does not speak English
  • The child is on an antidepressant medication, because it may complicate neuroimaging interpretation

Are you a good fit?

Simplified highlights. The study team always confirms the full details with you.

  • Adults roughly 7–12
  • Have Depression

What to expect, step by step

  1. 1

    Usually a few weeks

    The study team checks whether the study is a good fit for you, with a visit and sometimes lab tests. You can ask any questions before deciding.

  2. 2

    Treatment

    If you join and choose to continue, you receive the study treatment and are watched closely by medical staff.

  3. 3

    Follow-up

    After treatment, the team checks on your health and confirms the visit schedule with you. You can leave the study at any point.

Has this treatment been tested before?

The study team can share what safety testing has been done so far.

What you need to know before you apply

What is this study testing?+

The goal of this interventional study is to compare the baseline neural mechanisms and parenting in depressed and non-depressed children and to examine baseline neural mechanisms and parenting as predictors of Family-Focused Treatment for Childhood-Depression (FFT-CD) outcomes. The main questions it aims to answer are: * What are differences between depressed and non-depressed participants on baseline neural and parenting indicators?

Is it safe? Who makes sure of that?+

This is a research study. Every study is reviewed and monitored by an independent ethics board (called an IRB) whose job is to protect participants, and care is overseen by licensed medical staff. You'll be told the known risks before you agree to anything, and you can stop at any time.

Will I get a placebo instead of the real treatment?+

Some studies compare a treatment against a placebo (an inactive version), and some don't. If this one does, the study team will explain your chances of receiving the active treatment before you decide. Nothing is hidden from you.

Do I have to stop taking my current medications?+

It depends on the study. Some let you stay on your current medications and some ask you to adjust them. Never stop a medication on your own — the study team will review everything with you first.

Does it cost anything? Will I be paid?+

Study-related care is provided at no cost to you. Some studies also pay for your time; the coordinator can tell you if this one does. You should never be asked to pay to take part.

Do I need insurance? Will anyone ask about my immigration status?+

No. You do not need health insurance to take part in a research study, and you will not be asked about your immigration status to join. Taking part is about whether you're a medical fit for the study.

What if English isn't my first language?+

You have the right to understand everything before you agree. Study sites can often provide materials or an interpreter in your language — you can ask the coordinator for one.

Is my information private?+

Yes. Your health information is only shared with the study sites you choose to be contacted by, and only to help match and enroll you. It is never sold, and you can ask us to delete it at any time.

Source: ClinicalTrials.gov · NCT06289010 · Locations: Massachusetts