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Behavioral Intervention

WE CARE for Patient Satisfaction (PROSWECARE Trial)

N/A
Waitlist Available
Led By Arvin Garg, MD, MPH
Research Sponsored by Boston Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1.5-,2-,and 2.5- years post-implementation of we care
Awards & highlights

PROSWECARE Trial Summary

This trial will help determine if providing families with resources can reduce stress and improve health outcomes.

Eligible Conditions
  • Basic Unmet Material Needs
  • Patient Satisfaction
  • Community Resources
  • Provider Referrals

PROSWECARE Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1.5-,2-,and 2.5- years post-implementation of we care
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1.5-,2-,and 2.5- years post-implementation of we care for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Provider Referrals for Unmet Material Needs at Visit
Receipt of Community Resources
Secondary outcome measures
Acceptability of WE CARE measured via questionnaires
Appropriate referrals made by providers
Appropriateness of WE CARE measured via questionnaire
+5 more

PROSWECARE Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Self-directed web-based WE CARE implementation armExperimental Treatment1 Intervention
WE CARE will be implemented in the study site using a web-based implementation strategy. 1. Participants will receive the WE CARE survey at health supervision visits; this survey will be used to identify unmet material needs. 2. Providers will be trained on WE CARE via web-based tools (e.g., web-based seminar) which will teach them how to review the survey and provide referrals (community resource information sheets) from a Family Resource Book located in each exam room
Group II: On-site WE CARE implementation armExperimental Treatment1 Intervention
WE CARE will be implemented in the study site using a facilitated "on-site" strategy. 1. Participants will receive the WE CARE survey at health supervision visits; this survey will be used to identify unmet material needs. 2. Providers will be trained on WE CARE via an on-site team which will teach them how to review the survey and provide referrals (community resource information sheets) from a Family Resource Book located in each exam room.
Group III: Usual Care-ControlActive Control1 Intervention
Participants in the usual care group will receive standard pediatric care.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
WE CARE
2019
N/A
~1880

Find a Location

Who is running the clinical trial?

Boston Medical CenterLead Sponsor
382 Previous Clinical Trials
867,527 Total Patients Enrolled
University of Massachusetts, WorcesterLead Sponsor
342 Previous Clinical Trials
974,738 Total Patients Enrolled
Pediatric Research in Office SettingsNETWORK
1 Previous Clinical Trials
60 Total Patients Enrolled

Media Library

WE CARE (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT02918435 — N/A
Patient Satisfaction Research Study Groups: Usual Care-Control, On-site WE CARE implementation arm, Self-directed web-based WE CARE implementation arm
Patient Satisfaction Clinical Trial 2023: WE CARE Highlights & Side Effects. Trial Name: NCT02918435 — N/A
WE CARE (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT02918435 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the size of this research study's participant pool?

"Affirmative. In accordance with the information posted on clinicaltrials.gov, this research endeavour is currently seeking participants to enroll. The initial posting date was October 7th 2019 and it has been updated as recently as December 13th 2021. This investigation requires 2520 people from a single centre for successful completion."

Answered by AI

Is this research open to individuals older than 45?

"As per the stipulations of this medical trial, minors aged 2 months and under 10 years are eligible to participate."

Answered by AI

What aim is this medical experiment attempting to achieve?

"This medical trial, assessed over a 3 month period post-index visit, is primarily looking to evaluate the number of Provider Referrals for Unmet Material Needs at Visit. Other secondary outcomes include gauging whether Discussion of Unmet Needs (e.g., food insecurity) occurred in the well-child care visits and assessing Patient satisfaction through the CAHPS Clinician and Group Survey (Child). Lastly, Care coordination will be measured via the National Survey of Children's Health (2016)."

Answered by AI

Is this a research program I am eligible to join?

"This trial seeks to involve 2520 participants aged between 2 months and 10 who have parental/guardian consent (the adult must be 18 or above). Additionally, children need to present for a health supervision visit in order to qualify."

Answered by AI

Does this medical experiment have any slots open for volunteers?

"Affirmative. According to clinicaltrials.gov, this trial first went live on 10/7/2019 and was most recently updated on 12/13/2021. Currently, the medical research project is searching for 2520 participants from 1 location to take part in the study."

Answered by AI
~340 spots leftby Apr 2025