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WithdrawnNCT07884604Updated Oct 20, 2026

Concussion Goody Bag Study

An observational study in Sports Related Concussion, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago. Withdrawn at 1 site in United States. Open to participants aged 6 Years to 17 Years. Per ClinicalTrials.gov, last updated 2026-10-20.

Sponsored by Ann & Robert H Lurie Children's Hospital of Chicago · Observational

Why this study was withdrawn
Poor feasibility of project recruitment and execution
Updated Oct 20, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
6 Years to 17 Years
Sex
All
01

Study summary

For the pilot study, thirty eligible participants will be provided a concussion goody bag at their initial concussion evaluation visit. Each goody bag consists of 12 items, with a letter briefly describing the intended purpose for each item. Each participant will listen to a scripted tutorial by the research personnel, explaining the goody bag and why they are receiving it. Per standard of care, participants will return to clinic within 1-2 weeks for a follow up visit, at which time, they will complete a short questionnaire to assess overall usefulness of the bag, as well as individual rankings on how often they used each specific item. If the participant did not use any items, they will complete an additional question, describing why that item was not used, for each unused item. Also, the participants will be asked if they felt any additional items would have been helpful to them. Investigators expect these questionnaires to provide valuable insight from our patient perspectives about post-concussion care.

02

Conditions studied

  • Sports Related Concussion

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Keywords

  • Concussion
03

In context

Brain Concussion

550 studies on the registry are indexed under Brain Concussion; 154 are open to participants now.

Browse Brain Concussion studies →

Lead sponsor

Ann & Robert H Lurie Children's Hospital of Chicago is the lead sponsor of 180 studies on the registry; 30 are open to participants now.

Of its 10 completed or terminated interventional studies of FDA-regulated products, 5 (50%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Participants will be recruited from concussion clinics at the institution main hospital and satellite clinics.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • has a sports related concussion
  • between the ages of 6-17 years
  • is presenting to our clinic within three weeks of the concussion

Exclusion criteria

Exclusion Criteria:

  • has a history of prior diagnosed concussion
  • has a history of headache (migraine or non-migraine)
  • has a history of learning disability
  • has Attention Deficit Disorder (ADD)
  • has a history of anxiety, depression, or bipolar mood disorder
  • is non-English speaking
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Evaluation of participant opinions on the usefulness of a concussion goody bag.

    Participants will be provided a concussion goody bag at their initial concussion evaluation visit. At a participant's return visit to clinic, they are surveyed on the overall usefulness of the goody-bag and it's contents. The survey utilizes a subjective scale. The scale of usefulness is measured from \[1-5\] with 1 being "Not Helpful" and 5 being "Very Helpful"

    Time frame: 3 weeks

07

Study locations

1 site
  • Ann and Robert H. Lurie Children's Hospital
    Chicago, Illinois 60611, United States
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 20, 2026
Show all 1 update
  1. Oct 20, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07884604
Responsible party
Sponsor
First posted
Oct 20, 2026
Start date
Oct 2015
Primary completion
May 2019 (estimated)
Completion
Dec 2019 (estimated)
Last update
Oct 20, 2026
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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