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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03421795
Enrollment
178
Registered
2018-02-05
Start date
2017-05-08
Completion date
2018-08-02
Last updated
2019-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Keywords

pain assessment/management, developmental disabilities, children, education, respite workers

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.

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.

Interventions

OTHERLet's Talk About Pain Training

See arm/group descriptions.

OTHERFamily Centered Care Training

See arm/group descriptions.

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
Society of Pediatric Psychology
CollaboratorUNKNOWN
Western University
CollaboratorOTHER
University of Guelph
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

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.

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).

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Within intervention group change from baseline in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - RevisedBaseline (within 30 minutes prior to start of training), Post (within 30 minutes after completion of training)Pain-related knowledge assessment
Within intervention group change (i.e., maintenance) from post in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - RevisedPost (within 30 minutes after completion of training), Follow-Up (approximately one month after training)Pain-related knowledge assessment
Between group difference in scores on Questionnaire for Understanding Pain in Individuals with Intellectual and Developmental Disabilities - RevisedPost (within 30 minutes after completion of training)Pain-related knowledge assessment

Secondary

MeasureTime frameDescription
Between group difference ratings of perceived confidence in pain assessment abilitiesPost (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.
Between group difference ratings of perceived confidence in pain management abilitiesPost (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.
Between group difference ratings of perceived skill in pain assessmentPost (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.
Between group difference ratings of perceived skill in pain managementPost (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.
Within intervention group change from baseline in ratings of the feasibility of pain assessmentBaseline (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.
Within intervention group change from baseline in ratings of the feasibility of pain managementBaseline (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.
Within intervention group change from baseline in ratings of perceived confidence in pain assessmentBaseline (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.
Within intervention group change from baseline in ratings of perceived skill in pain assessmentBaseline (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.
Within intervention group change from baseline in ratings of perceived skill in pain managementBaseline (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.
Within intervention group change (i.e., maintenance) from post in ratings of the feasibility of pain assessmentPost (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.
Within intervention group change (i.e., maintenance) from post in ratings of the feasibility of pain managementPost (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.
Within intervention group change (i.e., maintenance) from post in ratings of perceived confidence in pain assessmentPost (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.
Within intervention group change (i.e., maintenance) from post in ratings of perceived confidence in pain managementPost (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.
Within intervention group change (i.e., maintenance) from post in ratings of perceived skill in pain assessmentPost (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.
Within intervention group change (i.e., maintenance) from post in ratings of perceived skill in pain managementPost (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.
Within intervention group change from baseline in ratings of perceived confidence in pain managementBaseline (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.
Between group difference in ratings of the feasibility of pain assessmentPost (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.
Between group difference ratings of the feasibility of pain managementPost (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.

Other

MeasureTime frameDescription
Between group difference in use of evidence-based pain assessment and management strategies as indicated on a researcher-generated questionnaire and in focus groupsFollow-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)
Within intervention group descriptive ratings of trainingPost (within 30 minutes after completion of training)Assessment of training program endorsement
Within intervention group change from baseline in use of evidence-based pain assessment and management strategies as indicated on a researcher-generated questionnaireBaseline (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)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026