Clinical Trials Logo

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
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05559255 - Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI N/A
Terminated NCT04356352 - Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain Phase 2/Phase 3
Completed NCT04748367 - Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care N/A
Completed NCT05057988 - Virtual Empowered Relief for Chronic Pain N/A
Completed NCT04466111 - Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
Recruiting NCT06206252 - Can Medical Cannabis Affect Opioid Use?
Completed NCT05868122 - A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy Phase 3
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Enrolling by invitation NCT06087432 - Is PNF Application Effective on Temporomandibular Dysfunction N/A
Completed NCT05508594 - Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 Phase 2/Phase 3
Recruiting NCT03646955 - Partial Breast Versus no Irradiation for Women With Early Breast Cancer N/A
Active, not recruiting NCT03472300 - Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
Completed NCT03678168 - A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries N/A
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Completed NCT03931772 - Online Automated Self-Hypnosis Program N/A
Completed NCT02913027 - Can We Improve the Comfort of Pelvic Exams? N/A
Terminated NCT02181387 - Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor? Phase 4
Recruiting NCT06032559 - Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment Phase 3
Active, not recruiting NCT03613155 - Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care