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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05698290
Other study ID # STUDY00007400
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date August 25, 2022
Est. completion date July 2025

Study information

Verified date April 2024
Source Michigan State University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this project is to develop and test the Helping Educators Learn Pediatric Pain Assessment & Intervention Needs (HELP Pain) program. HELP Pain provides training for school providers (e.g., school nurses, mental health professionals) on strategies to assess and manage pain-related concerns in school children. Participants will learn cognitive behavioral therapy techniques to help school children manage pain, and report on their use of strategies, and child's progress throughout the school year. Follow-up data will be collected in year 2.


Description:

Chronic pain is common among school children, and impacts social, emotional and academic functioning. School providers are often tasked with addressing student pain, but may have limited training in evidence-based pain management strategies. Thus, the PI developed a training program, HELP Pain, to train school providers, such as school nurses and mental health professionals, in cognitive behavioral therapy strategies for addressing student pain. In this study, the feasibility and acceptability of the training program will be evaluated. Provider knowledge will be evaluated before and after receiving the HELP Pain training. Further, the use of HELP Pain strategies with students and their associated disability and pain outcomes will be evaluated. Results will help to tailor the HELP Pain training program for future use.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 68
Est. completion date July 2025
Est. primary completion date July 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - engaged as a school provider in Michigan

Study Design


Related Conditions & MeSH terms


Intervention

Other:
HELP Pain Training Program
A training program to teach school providers nonpharmacologic (e.g., cognitive behavioral and mindfulness meditation) strategies to use with students with pain symptoms.

Locations

Country Name City State
United States Michigan State University Grand Rapids Michigan

Sponsors (1)

Lead Sponsor Collaborator
Michigan State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Child Functional Disability Inventory (FDI) Administration of the FDI to students is optional. The FDI is used to assess impairment due to pain over the past several days, and uses a Likert scale (0-4) to result in a score 0-60, where 60 implies decreased functioning. 9 months, 2 years
Other Child Pain Ratings - Numerical Scale Administration of the child pain ratings to students is optional. Highest, lowest, average and current pain over the past week are reported by a child to the provider using a numerical scale. The numerical scale is 0-10, with 10 indicating worse pain. 9 months, 2 years
Other Child Pain Ratings - Faces Scale Administration of the child pain ratings to students is optional. Highest, lowest, average and current pain over the past week are reported by a child to the provider using a faces scale. The faces scale contains 6 faces with scores of 0, 2, 4, 6, 8, or 10 respectively from left to right, where the rightmost face or score of 10 indicates worse pain. 9 months, 2 years
Other Child School Attendance Reporting of a child's school attendance is optional. School attendance, late arrivals, and early dismissal in one month (due to pain or other reasons), and school nurse visits for pain or other reasons (scheduled and unscheduled) as reported by the school provider specific to a child. 9 months, 2 years
Primary Feasibility - Qualitative report Implementation success of the program measured by a semi-structured qualitative interview method which addresses feasibility. 9 months
Primary Acceptability - Qualitative report Implementation success of the program measured by a semi-structured qualitative interview method which addresses acceptability. 9 months
Primary Appropriateness - Qualitative report Implementation success of the program measured by a semi-structured qualitative interview method which addresses appropriateness. 9 months
Primary Implementation Success - Quantitative report Twelve psychometrically validated items to assess program implementation success, will be administered after training. Providers will rate items with responses using a 5-point Likert scale ranging from strongly disagree (1) to strongly agree (5). 9 months
Secondary Knowledge Knowledge quiz scores before and after training, 0-20, where 20 indicates higher knowledge. 9 months
Secondary Fidelity Self-reported use of HELP Pain strategies with students via online survey. 9 months, 2 years
Secondary Self-report Knowledge Self-reported agreeableness using a 5-point Likert scale from strongly disagree (1) to strongly agree (5) to 3 statements indicating knowledge from the program. 9 months
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