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

NCT04499937 · ClinicalTrials.gov registry record · NA

ReCoUPS: Post-Concussion Patient Reports

A NA study, sponsored by Children's Hospital of Philadelphia.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT04499937: Completed NA study, sponsored by Children's Hospital of Philadelphia.

NCT04499937 is a NA study that has completed, run by Children's Hospital of Philadelphia. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04499937, a NA study, has completed, sponsored by Children's Hospital of Philadelphia.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

Physical and cognitive rest are recommended as treatment for concussion, but debate persists about the utility of this recommendation for patients recovering from concussion. In addition, patient adherence to physical and cognitive rest recommendations after concussion remains unknown. This study will measure and compare symptom and activity reports in the days and weeks after a concussion among patients randomly assigned to different incentive-based arms.

Primary Outcome

This is a study where each participant is sent a short survey (PCSI instrument) three times each day for 21 days. The participant is instructed to reply to each survey within several minutes of receiving the prompt. We are interested in the extent to which participants will adhere to this instruction. Therefore, the outcome of interest is whether or not the participant replied to a given survey prompt. When we evaluate patient adherence in the data, we do this by calculating the % of survey prom

Interventions

  • BEHAVIORAL Streak incentive
  • BEHAVIORAL Loss-based incentive
  • BEHAVIORAL Flat-fee control status quo condition
  • BEHAVIORAL Flat-Fitbit control status quo condition

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2019-03-03
Est. Completion 2021-02-05
Phase NA
Children's Hospital of Philadelphia

431 total trials

What the finished NCT04499937 record still lists

NCT04499937 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 4 interventions - of which Streak incentive is the first listed.

NCT04499937 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04499937 about?

NCT04499937 is a clinical study titled "ReCoUPS: Post-Concussion Patient Reports". Physical and cognitive rest are recommended as treatment for concussion, but debate persists about the utility of this recommendation for patients recovering from concussion. In addition, patient adherence to physical and cognitive rest recommendations after concussion remains unknown. This study wi...

What is the current status of trial NCT04499937?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2019-03-03. Estimated completion is 2021-02-05.

What interventions are being tested in trial NCT04499937?

The interventions under investigation include: Streak incentive (BEHAVIORAL), Loss-based incentive (BEHAVIORAL), Flat-fee control status quo condition (BEHAVIORAL), Flat-Fitbit control status quo condition (BEHAVIORAL).

Who is sponsoring clinical trial NCT04499937?

This trial is sponsored by Children's Hospital of Philadelphia, which has 431 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04499937's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 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

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

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 NCT04499937, the US trial registry maintained by the National Library of Medicine. NCT04499937 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.