Effectiveness of a Pain Assessment and Management Program for Respite Workers Supporting Children With Disabilities

Sponsor
University of Guelph (Other)
Overall Status
Completed
CT.gov ID
NCT03421795
Collaborator
Canadian Institutes of Health Research (CIHR) (Other), Society of Pediatric Psychology (Other), Western University (Other)
178
1
2
14.8
12

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Let's Talk About Pain Training
  • Other: Family Centered Care Training
N/A

Detailed Description

Background Information: Everyday pain is common in children with intellectual/developmental disabilities (I/DD). Inadequately managed pain in this population is a common problem, and this is likely due to these children's inability to communicate pain effectively. Unfortunately, many of these children are unable to accurately self-report or effectively communicate the pain experience. Thus, caregivers are often responsible for assessing their pain. Research has focused on professionals and parents, but it is also common for children with I/DD to receive care from others including respite workers. The investigators recently found a difference between pain beliefs held by respite workers and individuals with little to no experience with this population. Specifically, respite workers believed that a significantly larger percentage of children with severe I/DD sensed less pain than typically developing children. This is contrary to research suggesting that children with I/DD have similar pain perception but communicate it differently (e.g., through idiosyncratic behaviours). Thus, it is possible that respite workers miss critical cues when children with I/DD are in pain. As such, the investigators have developed and successfully piloted a pain training program targeted to respite workers who support children with I/DD. This program demonstrated initial success in improving respite workers' pain-related knowledge, as well as their perceptions of the feasibility of and their own confidence and skill in pain assessment and management with this population of children.

Within a randomized control trial, the objectives of this study are to further test the effectiveness of the Let's Talk About Pain respite worker training program on respite workers' (a) pain-related knowledge, (b) self-rated perceptions of the feasibility of and their own confidence and skill in pain assessment and management, and (c) use of pain assessment and management strategies specific to children with I/DD in respite settings. Participants will complete questionnaires immediately before and after provision of a pain training (or control training). Approximately one month after the training, participants will complete these questionnaires for a third time and participate in a focus group regarding their pain assessment and management strategy use.

The long term objectives of this line of research are to: 1) increase pain assessment and management abilities of respite workers, and, consequently, 2) decrease levels of suffering and ill-managed pain in children with I/DD.

Study Design

Study Type:
Interventional
Actual Enrollment :
178 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This is a multi-centre clustered parallel RCT with an intervention group (pain training) and control group (control training about family centered care, with an option to receive pain training after follow-up).This is a multi-centre clustered parallel RCT with an intervention group (pain training) and control group (control training about family centered care, with an option to receive pain training after follow-up).
Masking:
None (Open Label)
Masking Description:
Organizations will not be made explicitly aware of whether they have been allocated as part of the control or experimental conditions. Organizations will be told, however, that if they are not assigned to the experimental group, they will be given the option to also have an additional training about pain in children with DD at the end of the study. They will also know about the topics of both training programs and the purpose of the study. Participants will only be told that the purpose of the study is to learn about the impact that training programs can have on respite workers' knowledge about caring for children with DD. However, given some of the information in the consent form (e.g., study title is "Let's Talk about Pain"), it is likely that the treatment condition is clear to participants.
Primary Purpose:
Other
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
Actual Study Start Date :
May 8, 2017
Actual Primary Completion Date :
Jul 3, 2018
Actual Study Completion Date :
Aug 2, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Let's Talk About Pain Training

Participants complete pre-, post- and follow-up measures, and receive a pain training program. The pain assessment and management training will be based on a training previously developed and piloted by Genik et al. (2017). The training will be facilitated by the same researcher (L.G.) throughout the study.

Other: Let's Talk About Pain Training
See arm/group descriptions.

Sham Comparator: Family Centered Care Training

Participants complete all of the same measures as those in the intervention, but receive a training about family centered care. This training will be facilitated by Andrea Cross (PhD Candidate) from CanChild and will be related to the F-words of childhood disability (function, family, fitness, fun, friends, future; Rosenbaum & Gorter, 2012) .

Other: Family Centered Care Training
See arm/group descriptions.

Outcome Measures

Primary Outcome Measures

  1. Within intervention group change from baseline in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised [Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)]

    Pain-related knowledge assessment

  2. Within intervention group change (i.e., maintenance) from post in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised [Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training)]

    Pain-related knowledge assessment

  3. Between group difference in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised [Post (within 30 minutes after completion of training)]

    Pain-related knowledge assessment

  4. Between group difference in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - Revised [Follow-Up (approximately one month after training)]

    Pain-related knowledge assessment

Secondary Outcome Measures

  1. Between group difference in ratings of the feasibility of pain assessment [Post (within 30 minutes after completion of training)]

    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.

  2. Between group difference in ratings of the feasibility of pain assessment [Follow-Up (approximately one month after training)]

    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.

  3. Between group difference ratings of the feasibility of pain management [Post (within 30 minutes after completion of training)]

    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.

  4. Between group difference ratings of the feasibility of pain management [Follow-Up (approximately one month after training)]

    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.

  5. Between group difference ratings of perceived confidence in pain assessment abilities [Post (within 30 minutes after completion of training)]

    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.

  6. Between group difference ratings of perceived confidence in pain assessment abilities [Follow-Up (approximately one month after training)]

    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.

  7. Between group difference ratings of perceived confidence in pain management abilities [Post (within 30 minutes after completion of training)]

    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.

  8. Between group difference ratings of perceived confidence in pain management abilities [Follow-Up (approximately one month after training)]

    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.

  9. Between group difference ratings of perceived skill in pain assessment [Post (within 30 minutes after completion of training)]

    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.

  10. Between group difference ratings of perceived skill in pain assessment [Follow-Up (approximately one month after training)]

    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.

  11. Between group difference ratings of perceived skill in pain management [Post (within 30 minutes after completion of training)]

    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.

  12. Between group difference ratings of perceived skill in pain management [Follow-Up (approximately one month after training)]

    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.

  13. Within intervention group change from baseline in ratings of the feasibility of pain assessment [Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)]

    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.

  14. Within intervention group change from baseline in ratings of the feasibility of pain management [Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)]

    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.

  15. Within intervention group change from baseline in ratings of perceived confidence in pain assessment [Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)]

    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.

  16. Within intervention group change from baseline in ratings of perceived confidence in pain management [Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)]

    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.

  17. Within intervention group change from baseline in ratings of perceived skill in pain assessment [Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)]

    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.

  18. Within intervention group change from baseline in ratings of perceived skill in pain management [Baseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)]

    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.

  19. Within intervention group change (i.e., maintenance) from post in ratings of the feasibility of pain assessment [Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training)]

    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.

  20. Within intervention group change (i.e., maintenance) from post in ratings of the feasibility of pain management [Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training)]

    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.

  21. Within intervention group change (i.e., maintenance) from post in ratings of perceived confidence in pain assessment [Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training)]

    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.

  22. Within intervention group change (i.e., maintenance) from post in ratings of perceived confidence in pain management [Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training)]

    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.

  23. Within intervention group change (i.e., maintenance) from post in ratings of perceived skill in pain assessment [Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training)]

    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.

  24. Within intervention group change (i.e., maintenance) from post in ratings of perceived skill in pain management [Post (within 30 minutes after completion of training), Follow-Up (approximately one month after training)]

    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.

Other Outcome Measures

  1. Between group difference in use of evidence-based pain assessment and management strategies as indicated on a researcher-generated questionnaire and in focus groups [Follow-Up (approximately one month after training)]

    Assessment of use of evidence-based pain assessment and management strategies (researcher generated questionnaire with open-ended responses and focus groups)

  2. Within intervention group change from baseline in use of evidence-based pain assessment and management strategies as indicated on a researcher-generated questionnaire [Baseline (within 30 minutes prior to start of training), Follow-Up (approximately one month after training)]

    Assessment of use of evidence-based pain assessment and management strategies (researcher generated questionnaire)

  3. Within intervention group descriptive ratings of training [Post (within 30 minutes after completion of training)]

    Assessment of training program endorsement

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Guelph Guelph Ontario Canada N1G2W1

Sponsors and Collaborators

  • University of Guelph
  • Canadian Institutes of Health Research (CIHR)
  • Society of Pediatric Psychology
  • Western University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Meghan McMurtry, Associate Professor, University of Guelph
ClinicalTrials.gov Identifier:
NCT03421795
Other Study ID Numbers:
  • REB16-12-696
First Posted:
Feb 5, 2018
Last Update Posted:
May 7, 2019
Last Verified:
May 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Meghan McMurtry, Associate Professor, University of Guelph
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 7, 2019