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

NCT05231837 · ClinicalTrials.gov registry record · Phase 3

Neighborhood Park Youth Sports Program Fee Waiver and Intensive Family Outreach

A Phase 3 study, sponsored by University of Minnesota.

Completed
Registry status
Phase 3
Development phase
430
Enrollment target

NCT05231837: Completed Phase 3 study, sponsored by University of Minnesota.

NCT05231837 is a Phase 3 study that has completed, run by University of Minnesota. The registered enrollment target is 430 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (44% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05231837, a Phase 3 study, has completed, sponsored by University of Minnesota.

COMPLETED
Registry status
Phase 3
Development phase
430 participants
Enrollment target

Study Summary

To evaluate a park-level intervention to increase child moderate/vigorous physical activity (MVPA), and decrease sedentary time among low-income racially/ethnically diverse children ages 6-12 yrs. Neighborhood parks (n=20) from Minneapolis (n=8) and Saint Paul (n=12) park systems will be randomized for a 2-year period to one of two arms: 1) Intensive Park Outreach and Youth Sports Program Fee Waiver (n=10); or 2) Youth Sports Program Fee Waiver Only (n=10). The evaluation cohort will consist of 432 children ages 6-12 yrs who reside in one of the 20 randomized park neighborhoods. Measurements from evaluation cohort-enrolled individual children will be collected at baseline, 6, 12, and 24 months.

Primary Outcome

Accelerometers worn for 7 day calculate minutes per day of moderate and vigorous physical activity

Interventions

  • BEHAVIORAL Experimental: Fee Waiver
  • BEHAVIORAL Fee Waiver Plus Intensive Outreach

Trial Details

FieldValue
Enrollment Target 430 participants
Start Date 2022-02-15
Est. Completion 2025-12-18
Phase Phase 3
University of Minnesota

966 total trials

What the finished NCT05231837 record still lists

NCT05231837 is an interventional study that assigns participants to a tested intervention. The registered 430 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (44% lower).

The record links to 0 conditions, and to 2 interventions - of which Experimental: Fee Waiver is the first listed.

NCT05231837 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05231837 about?

NCT05231837 is a clinical study titled "Neighborhood Park Youth Sports Program Fee Waiver and Intensive Family Outreach". To evaluate a park-level intervention to increase child moderate/vigorous physical activity (MVPA), and decrease sedentary time among low-income racially/ethnically diverse children ages 6-12 yrs. Neighborhood parks (n=20) from Minneapolis (n=8) and Saint Paul (n=12) park systems will be randomized ...

What is the current status of trial NCT05231837?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 430 participants. The study started on 2022-02-15. Estimated completion is 2025-12-18.

What interventions are being tested in trial NCT05231837?

The interventions under investigation include: Experimental: Fee Waiver (BEHAVIORAL), Fee Waiver Plus Intensive Outreach (BEHAVIORAL).

Who is sponsoring clinical trial NCT05231837?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05231837's enrollment target sits among peer trials

430 877th of 2000 higher than 1,123 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

  • NCT05327023 · 430 participants · Phase 1

    Donor Lymphocyte Infusion After Allogeneic Hematopoietic Cell Transplantation for High-Risk Hematologic Malignancies

  • NCT05457985 · 430 participants · NA

    Testing Adaptive Interventions to Improve Posttraumatic Stress Disorder Treatment Outcomes in Federally Qualified Health Centers

  • NCT05532982 · 430 participants

    Parkinson's Disease in Asian Americans

  • NCT05844891 · 430 participants · NA

    Telehealth-Enhanced Asthma Care for Home After the Emergency Room

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05231837, the US trial registry maintained by the National Library of Medicine. NCT05231837 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.