Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00867802 · ClinicalTrials.gov registry record · NA

Mindfulness Intervention For Child Abuse Survivors (MICAS)

A NA study of Child Abuse Survivors, sponsored by University of Maryland, Baltimore.

Completed
Registry status
NA
Development phase
20
Enrollment target
1
Study location

NCT00867802: Completed NA study of Child Abuse Survivors, sponsored by University of Maryland, Baltimore.

NCT00867802 is a NA study of Child Abuse Survivors that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00867802, a NA study of Child Abuse Survivors, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to assess the effect of meditation training called Mindfulness-Based Stress Reduction on reducing the symptoms of psychological distress among adult survivors of child abuse.

Conditions Studied

Interventions

  • BEHAVIORAL Mindfulness-Based Stress Reduction program

Study Locations (1)

Maryland

  • Kernan Hospital - Baltimore

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2007-05
Est. Completion 2009-03
Phase NA
University of Maryland, Baltimore

560 total trials

What the finished NCT00867802 record still lists

NCT00867802 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Child Abuse Survivors appearing as the primary indexed condition, and to 1 intervention - of which Mindfulness-Based Stress Reduction program is the first listed.

NCT00867802 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT00867802 about?

NCT00867802 is a clinical study titled "Mindfulness Intervention For Child Abuse Survivors (MICAS)". The purpose of this study is to assess the effect of meditation training called Mindfulness-Based Stress Reduction on reducing the symptoms of psychological distress among adult survivors of child abuse.

What is the current status of trial NCT00867802?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2007-05. Estimated completion is 2009-03.

What conditions does trial NCT00867802 study?

This clinical trial studies the following conditions: Child Abuse Survivors.

What interventions are being tested in trial NCT00867802?

The interventions under investigation include: Mindfulness-Based Stress Reduction program (BEHAVIORAL).

Who is sponsoring clinical trial NCT00867802?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00867802 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT00867802's enrollment target sits among peer trials

20 1768th of 2000 higher than 140 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00867802, the US trial registry maintained by the National Library of Medicine. NCT00867802 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.