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

NCT01182051 · ClinicalTrials.gov registry record · NA

A Study of Family-based Cognitive-behavioral Therapy for Chronic Pediatric Headache and Anxiety

A NA study, sponsored by Johns Hopkins University.

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT01182051: Completed NA study, sponsored by Johns Hopkins University.

NCT01182051 is a NA study that has completed, run by Johns Hopkins University. The registered enrollment target is 15 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01182051, a NA study, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

The primary aim of this proposal is to refine the intervention under investigation (i.e., family-based CBT) and evaluate the feasibility and acceptability of the intervention and methods (e.g., recruitment, assessments). The secondary aim of this proposal is to compare the relative efficacy of an 8 session family-based cognitive-behavioral therapy (CBT) to Relaxation Training (RT) for reducing anxiety and chronic headaches in youth (N = 30) ages 7-17 years. It is hypothesized that CBT will result in greater reductions in both anxiety and headache frequency and severity compared to RT.

Primary Outcome

Youth and parents will complete a daily headache and anxiety diary to track the frequency and severity of headaches and anxiety symptoms. In addition, the diary will assess medication use, missed school/activities, as well as antecedents and consequences.

Interventions

  • BEHAVIORAL CBT or relaxation training

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2010-03
Est. Completion 2012-06
Phase NA
Johns Hopkins University

1,448 total trials

What the finished NCT01182051 record still lists

NCT01182051 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 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 0 conditions, and to 1 intervention - of which CBT or relaxation training is the first listed.

NCT01182051 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01182051 about?

NCT01182051 is a clinical study titled "A Study of Family-based Cognitive-behavioral Therapy for Chronic Pediatric Headache and Anxiety". The primary aim of this proposal is to refine the intervention under investigation (i.e., family-based CBT) and evaluate the feasibility and acceptability of the intervention and methods (e.g., recruitment, assessments). The secondary aim of this proposal is to compare the relative efficacy of an 8...

What is the current status of trial NCT01182051?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2010-03. Estimated completion is 2012-06.

What interventions are being tested in trial NCT01182051?

The interventions under investigation include: CBT or relaxation training (BEHAVIORAL).

Who is sponsoring clinical trial NCT01182051?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01182051's enrollment target sits among peer trials

15 1881st of 2000 higher than 92 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

  • NCT01889381 · 15 participants · Phase 2

    Human Craniomaxillofacial Allotransplantation

  • NCT02530073 · 15 participants · NA

    Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) for CDH

  • NCT02535936 · 15 participants · NA

    Cortical Plasticity in Spastic Diplegia After Selective Dorsal Rhizotomy

  • NCT02918474 · 15 participants · NA

    Decision Making Tool in Supporting Decision Making in Contralateral Prophylactic Mastectomy in Patients With Newly Diagnosed Breast Cancer

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 NCT01182051, the US trial registry maintained by the National Library of Medicine. NCT01182051 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.