Pain Clinical Trial
Official title:
Let's Talk About Pain: A Randomized Controlled Trial Testing the Effectiveness of a Pain Assessment and Management Training Program for Respite Workers Supporting Children With Intellectual and Developmental Disabilities
NCT number | NCT03421795 |
Other study ID # | REB16-12-696 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 8, 2017 |
Est. completion date | August 2, 2018 |
Verified date | May 2019 |
Source | University of Guelph |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study investigates the impact of pain training delivery for respite care providers who support children with developmental disabilities on (a) pain assessment and management-related knowledge, (b) participant self-rated perceptions of the feasibility, confidence and skill in pain assessment and management, and (c) strategy use. Half of the participants will receive the pain training, while half will receive the training about family-centered care, and be offered the pain training after completion of the follow-up.
Status | Completed |
Enrollment | 178 |
Est. completion date | August 2, 2018 |
Est. primary completion date | July 3, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Over the age of 18 - Proficient in the English language - Active respite worker who provides respite care to children (age 0 - 18) with developmental disabilities Exclusion Criteria: - n/a |
Country | Name | City | State |
---|---|---|---|
Canada | University of Guelph | Guelph | Ontario |
Lead Sponsor | Collaborator |
---|---|
University of Guelph | Canadian Institutes of Health Research (CIHR), Schulich School of Medicine & Dentistry, Western University, Society of Pediatric Psychology |
Canada,
Breau LM, MacLaren J, McGrath PJ, Camfield CS, Finley GA. Caregivers' beliefs regarding pain in children with cognitive impairment: relation between pain sensation and reaction increases with severity of impairment. Clin J Pain. 2003 Nov-Dec;19(6):335-44. — View Citation
Chen-Lim ML, Zarnowsky C, Green R, Shaffer S, Holtzer B, Ely E. Optimizing the assessment of pain in children who are cognitively impaired through the quality improvement process. J Pediatr Nurs. 2012 Dec;27(6):750-9. doi: 10.1016/j.pedn.2012.03.023. Epub 2012 Apr 10. Review. — View Citation
Dubois A, Capdevila X, Bringuier S, Pry R. Pain expression in children with an intellectual disability. Eur J Pain. 2010 Jul;14(6):654-60. doi: 10.1016/j.ejpain.2009.10.013. Epub 2009 Dec 5. — View Citation
Genik LM, McMurtry CM, Breau LM, Lewis SP, Freedman-Kalchman T. Pain in Children With Developmental Disabilities: Development and Preliminary Effectiveness of a Pain Training Workshop for Respite Workers. Clin J Pain. 2018 May;34(5):428-437. doi: 10.1097/AJP.0000000000000554. — View Citation
Genik LM, McMurtry CM, Breau LM. Caring for children with intellectual disabilities part 1: Experience with the population, pain-related beliefs, and care decisions. Res Dev Disabil. 2017 Mar;62:197-208. doi: 10.1016/j.ridd.2017.01.020. Epub 2017 Feb 14. — View Citation
Twycross A, Williams A. Establishing the validity and reliability of a pediatric pain knowledge and attitudes questionnaire. Pain Manag Nurs. 2013 Sep;14(3):e47-53. doi: 10.1016/j.pmn.2011.03.001. Epub 2011 Apr 17. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Between group difference in use of evidence-based pain assessment and management strategies as indicated on a researcher-generated questionnaire and in focus groups | Assessment of use of evidence-based pain assessment and management strategies (researcher generated questionnaire with open-ended responses and focus groups) | Follow-Up (approximately one month after training) | |
Other | Within intervention group change from baseline in use of evidence-based pain assessment and management strategies as indicated on a researcher-generated questionnaire | Assessment of use of evidence-based pain assessment and management strategies (researcher generated questionnaire) | Baseline (within 30 minutes prior to start of training), Follow-Up (approximately one month after training) | |
Other | Within intervention group descriptive ratings of training | Assessment of training program endorsement | Post (within 30 minutes after completion of training) | |
Primary | Within intervention group change from baseline in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised | Pain-related knowledge assessment | Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training) | |
Primary | Within intervention group change (i.e., maintenance) from post in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised | Pain-related knowledge assessment | Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training) | |
Primary | Between group difference in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised | Pain-related knowledge assessment | Post (within 30 minutes after completion of training) | |
Primary | Between group difference in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised | Pain-related knowledge assessment | Follow-Up (approximately one month after training) | |
Secondary | Between group difference in ratings of the feasibility of pain assessment | Researcher generated scale measuring participants' perceptions of the feasibility of pain assessment; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training) | |
Secondary | Between group difference in ratings of the feasibility of pain assessment | Researcher generated scale measuring participants' perceptions of the feasibility of pain assessment; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Follow-Up (approximately one month after training) | |
Secondary | Between group difference ratings of the feasibility of pain management | Researcher generated scale measuring participants' perceptions of the feasibility of pain management; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training) | |
Secondary | Between group difference ratings of the feasibility of pain management | Researcher generated scale measuring participants' perceptions of the feasibility of pain management; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Follow-Up (approximately one month after training) | |
Secondary | Between group difference ratings of perceived confidence in pain assessment abilities | Researcher generated scale measuring participants' perceptions of their own confidence in their pain assessment abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training) | |
Secondary | Between group difference ratings of perceived confidence in pain assessment abilities | Researcher generated scale measuring participants' perceptions of their own confidence in their pain assessment abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Follow-Up (approximately one month after training) | |
Secondary | Between group difference ratings of perceived confidence in pain management abilities | Researcher generated scale measuring participants' perceptions of their own confidence in their pain management abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training) | |
Secondary | Between group difference ratings of perceived confidence in pain management abilities | Researcher generated scale measuring participants' perceptions of their own confidence in their pain management abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Follow-Up (approximately one month after training) | |
Secondary | Between group difference ratings of perceived skill in pain assessment | Researcher generated scale measuring participants' perceptions of their own skill in pain assessment; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training) | |
Secondary | Between group difference ratings of perceived skill in pain assessment | Researcher generated scale measuring participants' perceptions of their own skill in pain assessment; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Follow-Up (approximately one month after training) | |
Secondary | Between group difference ratings of perceived skill in pain management | Researcher generated scale measuring participants' perceptions of their own skill in pain management; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training) | |
Secondary | Between group difference ratings of perceived skill in pain management | Researcher generated scale measuring participants' perceptions of their own skill in pain management; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Follow-Up (approximately one month after training) | |
Secondary | Within intervention group change from baseline in ratings of the feasibility of pain assessment | Researcher generated scale measuring participants' perceptions of the feasibility of pain assessment; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training) | |
Secondary | Within intervention group change from baseline in ratings of the feasibility of pain management | Researcher generated scale measuring participants' perceptions of the feasibility of pain management; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training) | |
Secondary | Within intervention group change from baseline in ratings of perceived confidence in pain assessment | Researcher generated scale measuring participants' perceptions of their own confidence in their pain assessment abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training) | |
Secondary | Within intervention group change from baseline in ratings of perceived confidence in pain management | Researcher generated scale measuring participants' perceptions of their own confidence in their pain management abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training) | |
Secondary | Within intervention group change from baseline in ratings of perceived skill in pain assessment | Researcher generated scale measuring participants' perceptions of their own skill in pain assessment; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training) | |
Secondary | Within intervention group change from baseline in ratings of perceived skill in pain management | Researcher generated scale measuring participants' perceptions of their own skill in pain management; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training) | |
Secondary | Within intervention group change (i.e., maintenance) from post in ratings of the feasibility of pain assessment | Researcher generated scale measuring participants' perceptions of the feasibility of pain assessment; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training) | |
Secondary | Within intervention group change (i.e., maintenance) from post in ratings of the feasibility of pain management | Researcher generated scale measuring participants' perceptions of the feasibility of pain management; 0 (Not feasible at all) - 10 (highly/extremely feasible) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training) | |
Secondary | Within intervention group change (i.e., maintenance) from post in ratings of perceived confidence in pain assessment | Researcher generated scale measuring participants' perceptions of their own confidence in their pain assessment abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training) | |
Secondary | Within intervention group change (i.e., maintenance) from post in ratings of perceived confidence in pain management | Researcher generated scale measuring participants' perceptions of their own confidence in their pain management abilities; 0 (Not confident at all) - 10 (highly/extremely confident) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training) | |
Secondary | Within intervention group change (i.e., maintenance) from post in ratings of perceived skill in pain assessment | Researcher generated scale measuring participants' perceptions of their own skill in pain assessment; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training) | |
Secondary | Within intervention group change (i.e., maintenance) from post in ratings of perceived skill in pain management | Researcher generated scale measuring participants' perceptions of their own skill in pain management; 0 (Not skilled at all) - 10 (highly/extremely skilled) Likert Scale. Higher scores are better. | Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training) |
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 | |
Completed |
NCT04748367 -
Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care
|
N/A | |
Terminated |
NCT04356352 -
Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain
|
Phase 2/Phase 3 | |
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
|