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

NCT01490619 · ClinicalTrials.gov registry record · NA

Resilience Promotion in Teens With Type 1 Diabetes: Preventing Negative Outcomes

A NA study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.

Completed
Registry status
NA
Development phase
280
Enrollment target

NCT01490619: Completed NA study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.

NCT01490619 is a NA study that has completed, run by Ann & Robert H Lurie Children's Hospital of Chicago. The registered enrollment target is 280 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01490619, a NA study, has completed, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.

COMPLETED
Registry status
NA
Development phase
280 participants
Enrollment target

Study Summary

Adolescents with type 1 diabetes are at increased risk for depressive symptoms, poor coping and problem-solving skills, poor regimen adherence, and negative diabetes-specific health outcomes. Although a handful of psychological interventions targeting adolescents' poor behavioral and emotional functioning demonstrate beneficial effects on disease management and outcomes, no prevention programs exist that equip adolescents with behavioral skills and cognitive strategies necessary to reduce these risks. Therefore, the proposed research will test whether a diabetes-specific adaptation of a resilience promoting, depression-prevention intervention for adolescents with type 1 diabetes will reduce both the risk of poor psychological functioning and the risk of negative health outcomes over time.

Primary Outcome

Investigators expect that Depressive symptoms will change over time. Specifically, it is expected that depressive symptoms will not increase and may even decrease in the Healthy Thinking in Teens arm, whereas depressive symptoms will increase in the Advanced Diabetes Education arm.

Interventions

  • BEHAVIORAL Healthy Thinking In Teens
  • OTHER Advanced Diabetes Education.

Trial Details

FieldValue
Enrollment Target 280 participants
Start Date 2011-10
Est. Completion 2018-03-30
Phase NA

What the finished NCT01490619 record still lists

NCT01490619 is an interventional study that assigns participants to a tested intervention. The registered 280 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 2 interventions - of which Healthy Thinking In Teens is the first listed.

NCT01490619 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01490619 about?

NCT01490619 is a clinical study titled "Resilience Promotion in Teens With Type 1 Diabetes: Preventing Negative Outcomes". Adolescents with type 1 diabetes are at increased risk for depressive symptoms, poor coping and problem-solving skills, poor regimen adherence, and negative diabetes-specific health outcomes. Although a handful of psychological interventions targeting adolescents' poor behavioral and emotional funct...

What is the current status of trial NCT01490619?

This trial is currently completed. It is a NA study. The enrollment target is 280 participants. The study started on 2011-10. Estimated completion is 2018-03-30.

What interventions are being tested in trial NCT01490619?

The interventions under investigation include: Healthy Thinking In Teens (BEHAVIORAL), Advanced Diabetes Education. (OTHER).

Who is sponsoring clinical trial NCT01490619?

This trial is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01490619's enrollment target sits among peer trials

280 380th of 2000 higher than 1,620 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

  • NCT04084730 · 280 participants · Phase 2

    Study of 3-Day Partial Breast Radiation Therapy in Women With Breast Cancer

  • NCT04518657 · 280 participants · NA

    Internet-Delivered Lifestyle Physical Activity Intervention for Cognitive Processing Speed in Multiple Sclerosis

  • NCT04634916 · 280 participants · NA

    Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF System

  • NCT04829617 · 280 participants · NA

    Promoting Well-being and Health in Heart Failure

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 NCT01490619, the US trial registry maintained by the National Library of Medicine. NCT01490619 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.