Knowledge, Attitudes, PracticeNCT04787081
Nighttime Postural Care: Caregiver Training Program and Outcome Measure Feasibility
A study testing Sleep Care Positioning Training Program GRP1 and Sleep Care Positioning Training Program GRP2 in people with Knowledge, Attitudes, Practice, run by St. Catherine University at 1 site in United States.
Trial summary
This experimental study investigated the feasibility of a sleep care positioning training protocol by comparing two educational interventions using a randomized control design. The overarching Population Intervention Comparison Outcomes (PICO) question was: Is the training protocol feasible for use in training… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Knowledge, Attitudes, Practice
- What is being tested?
- Sleep Care Positioning Training Program GRP1 and Sleep Care Positioning Training Program GRP2
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 38 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Jun 2018to 22 Sep 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Professional and non-professional caregivers of children with movement disorders or cerebral palsy.
Who cannot join
- Caregivers without knowledge of sleep habits and routines of persons with such diagnoses
Trial locations and contacts
1 site in 1 country.
United States1 site
St. Catherine University
Saint Paul, Minnesota, 55105
About this study
This experimental study investigated the feasibility of a sleep care positioning training protocol by comparing two educational interventions using a randomized control design. The overarching Population Intervention Comparison Outcomes (PICO) question was: Is the training protocol feasible for use in training caregivers? Question one includes the following sub questions: A. Is there a difference in perceived competence to implement aspects of nighttime postural care intervention or observed ability to position the person in a sleep system between caregivers receiving one training program versus another? B. Does the training protocol prepare caregivers to implement nighttime postural care (NTPC).
Read the detailed description
Target Population
Investigators planned to recruit a convenience sample of 40 adult participants identified as professional or non-professional care providers (primarily from two community organizations that specialize in serving clients with CP). Care providers of children (aged 6-12) with severe CP (those with limited ability to move and/or whom require use of a wheelchair) were the primary target population, since this matches the intended sample of a future intervention study. However caregivers of children outside of the 6-12 age range whom were candidates for NTPC and had similar mobility limitations as those with severe CP would not be excluded. Professional care providers could be nurses, occupational and physical therapists, assistive technology providers, etc. Non-professional care providers could be family members, care attendants, etc. Only individuals with knowledge of the child's sleep habits or routines were to be included in the study
Investigators used a mixed methods double-blind parallel group design, randomly assigning a consecutive sample of adults to an educational intervention (Lesson A or Lesson B).
Participant Recruitment
Investigators emailed flyers, recruiting participants from clinics serving persons with CP and universities educating healthcare providers and included professional and non-professional caregivers of persons with movement disorders, primarily CP with knowledge of a child's sleep habits and routines.
Participant activities
Participants completed study activities on one scheduled date: Consent process, baseline questionnaire (immediately before training), online education, post-training questionnaire, positioning of a simulated "client", post-simulation questionnaire, and exit interview. Participants completing all aspects of the study received a $50 gift card.
Randomization and blinding
The Principal Investigator (PI) enrolled participants, designating subject numbers and professional or non-professional labels. The research assistant completed randomization, drawing concealed numbers from an envelope, using Zelen's model of co-variate adaptive group randomization, and applying a threshold difference of three to balance professionals and non-professionals. An information technologist registered participants into their assigned lesson. At most five participants at a time were allowed in a classroom, with each room assigned a single lesson (A or B). Research assistants instructed participants on accessing and navigating their lesson and keeping details confidential. These processes helped ensure the PI, participants, and clinician simulation raters were not informed of lesson assignment.
Participants had the option to complete the non-assigned lesson in addition to their assigned lesson. Investigators verified participants' completion of all research activities (besides the exit interview) before the optional non-assigned lesson.
Intervention similarities and differences
Both online lessons included modules on evidence for NTPC, risk factor monitoring, sleep system types and set up, positioning methods, and outcome measures and were delivered via D2L Brightspace, a cloud-based learning management system. Both lessons' positioning-methods modules included video-based instruction. Lesson formats differed by source and design: Lesson A, created by a university's postural-care scholars using Camtasia® video creation software, consisted of interactive videos embedded with learning checkpoints, while Lesson B included written summary statements and links to freely available web-based information.
Simulation
Following their lesson and post-training questionnaire, participants positioned a "client" in a hospital bed using a designated commercial sleep system (henceforth termed "simulation"). The investigators followed protocols, instructing that participants position the client to the best of their ability, not using notes or asking observers for help; the "client" be positioned using straps to facilitate tight hamstrings in an asymmetrical-lying position common for persons with CP (i.e. head turned left, legs windswept right and knee flexed); and the clinician raters should complete the room set-up with the bed centered against the north wall, sleep system parts arranged consistently on a designated table, and that they should sit at predetermined observational locations.
Simulation raters
Health practitioners (two at a time) serving as clinician raters used the simulation observation instrument, independently observing and documenting a participant's positioning skills. An assistive technology professional and occupational therapist served as primary raters, rating 30 and 29 participants, respectively. Two secondary raters (both occupational therapists, one the PI) completed the remaining observations.
Data collection measures
Investigators collected quantitative and qualitative data using questionnaires for obtaining participants' self-perceptions of competence and lesson feedback. An observation instrument was used for scoring and describing participants' simulation performance. Fieldnotes were used for recording participant activities across the study period. The PI designed all study instruments, after reviewing competency literature, conducting a pilot study (unpublished) and consulting an academic measurement expert.
Statistical power
Before data collection, investigators chose a significance level (0.05) with plans for enrolling a minimum of 30 participants. With 15 participants per group, so there would be 80% power to detect a difference between groups of 1.06 standard deviations, where "standard deviation" describes variation within groups (i.e., Cohen's d = 1.06). Because this is the first study examining caregivers' NTPC competence from online education, no prior data could inform power calculation or supply a "standard deviation" value.
Data analysis, quantitative outcomes
Perceived Competence. Each participant provided a total average perceived competence score (total average from knowledge, ability and confidence sub-scores) at three times: baseline, post-training, and post-simulation. Investigators analyzed these scores using a mixed linear model; the random effect was participant, and fixed effects were group (Lesson A or Lesson B), professional vs. non-professional status, time (baseline, post-training, and post-simulation), and all two-way and three-way interactions. Investigators tested change over time within groups using a contrast in the group-by-time interaction (which combines professionals and non-professionals) and compared groups at each time also using contrasts in the group-by-time interaction. Statistical analyses used JMP (v. 14.0.0 Pro, SAS Institute, Cary NC).
Observed competence. Investigators computed participants' average positioning/simulation score (number correct out of 16 tasks from the simulation observation instrument) and used a mixed linear model to examine differences in observed positioning ability based on group (Lesson A or B) and professional vs. non-professional status.
Correlation of perceived and observed competence. Investigators used Pearson's correlation (r) to measure the association between participants' average self-ratings on positioning-based competence items and their average correct positioning/simulation scores, to understand the groups' ability to self-assess performance.
Interrater Reliability. Investigators measured interrater reliability using the intra-class correlation (ICC), once including all simulation observation raters and separately including the two primary clinician raters and the PI.
Data analysis, qualitative
For qualitative data, investigators used a modified grounded theory approach of open, axial and selective coding similar to that described by Bhattacherjee. From questionnaire and exit interview data, the PI read line-by-line, coding responses into categories and themes. From the simulation observation instrument, the PI listed each participant's incorrectly completed tasks and used a table to organize those tasks most frequently missed or completed incorrectly. Then clinicians' descriptive statements corresponding to incorrectly completed tasks were tabulated and reviewed line-by-line and coded into categories and themes.
Note: In addition to the above stated plan for examining the feasibility of the sleep care positioning training program, investigators also planned to examine the internal consistency reliability of the sleep disturbance scale for children (SDSC), a 27-item inventory rated on a 5 point Likert-type scale which was created by Bruni et al in 1996. To examine its reliability, study participants who self-identified as having night to night knowledge of a child with cerebral palsy's sleep performance were asked to complete the SDSC. While data was collected for this aspect of the study, only 10 participants self-identified as having such knowledge; thus, further analysis of the tools' reliability was not completed by investigators.
- Conditions
- Knowledge, Attitudes, Practice
- Being tested
- Sleep Care Positioning Training Program GRP1, Sleep Care Positioning Training Program GRP2
- Keywords
- competence post learning, nighttime postural care education, online caregiver education, postural care, cerebral palsy, sleep positioning
- Medical subject headings
- Behavior, Cerebral Palsy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Sleep Care Positioning Training Program GRP1Other
Also called Lesson A
Video-based tutorial covering six nighttime postural care topic areas which contained narration and closed captioning. This 2-hour online training program was delivered in a University classroom via D2L Brightspace.
Sleep Care Positioning Training Program GRP2Other
Also called Lesson B
Web-link based tutorial covering six nighttime postural care topic areas which contained mostly written content. This self-paced online training program was delivered in a University classroom via D2L Brightspace.
| Study group | Role | What they receive |
|---|---|---|
| Sleep Care Positioning Training Program GRP1 | Experimental | A sleep care positioning lesson created by a University's postural-care scholars using Camtasia® video creation software with modules on evidence for night-time postural care, risk factor monitoring, sleep system types and set up, positioning methods, and outcome measures. This lesson consisted of interactive videos embedded with learning checkpoints. All videos included narration and closed captioning. The following link contains the videos which were modified post-study to reflect some of the participant's feedback: https://stkatentpc.weebly.com/ Receives: Other: Sleep Care Positioning Training Program GRP1 |
| Sleep Care Positioning Training Program GRP2 | Active comparator | A sleep care positioning lesson created by a research assistant along with the principal investigator with modules on evidence for night-time postural care, risk factor monitoring, sleep system types and set up, positioning methods, and outcome measures. This lesson consisted of primarily written summary statements and links to freely available web-based information. Most of this lesson's modules included written information that the participant would need to read with the exception of the positioning methods modules. For the positioning module, participants were provided with links to manufacturers' websites which contained video clips on how to place postural supports. Receives: Other: Sleep Care Positioning Training Program GRP2 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Baseline Sleep Care Positioning Questionnaire
Perceived competence questionnaire with 4-pt. ratings of knowledge, ability and confidence for nighttime postural care research, risk factor monitoring, sleep system types / set-up, positioning a person, and measuring outcomes.
Measured: Completed immediately before training/educational intervention. Same day as training.
Post Sleep Care Positioning Program Questionnaire
Perceived competence questionnaire with 4-pt. ratings of knowledge, ability and confidence for nighttime postural care research, risk factor monitoring, sleep system types / set-up, positioning a person, and measuring outcomes.
Measured: Completed immediately after training / educational intervention. Same day as training.
Post Simulation Sleep Care Positioning Program Questionnaire
Perceived competence questionnaire with 4-pt. ratings of knowledge, ability and confidence for nighttime postural care research, risk factor monitoring, sleep system types / set-up, positioning a person, and measuring outcomes.
Measured: Completed immediately after simulation activity, after positioning a person in a sleep system. Same day as training.
Secondary outcomes (1)
Simulation Observation Instrument
Instrument with list of 16 positioning tasks with Yes/No columns meant for raters to check for each task, indicating whether or not task was completed by participant. Additionally this instrument included space and directions for raters to record observations of participants from the start to end of the simulation/positioning the person activity.
Measured: Completed after training and post-training questionnaire. Same day as training.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Mar 2021
- Study start1 Jun 2018
- Primary completion22 Sep 2018
- Study completion22 Sep 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Knowledge, Attitudes, PracticeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Mixed methods double-blind parallel group design, involving a consecutive sample of adults being randomly assigned to an educational intervention (Group A or B). The Principal Investigator enrolled participants, designating subject numbers and professional or non-professional labels. The research assistant completed randomization, drawing concealed numbers from an envelope to determine participant's educational intervention group (A or B). To balance the number of professionals and non-professionals across groups, the research assistant used co-variate adaptive group randomization and applied a difference threshold of 3.
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 38 participants (actual)
Sponsor and investigators
- Lead sponsor
- St. Catherine University
- Sponsor type
- University, hospital or other
- Collaborators
- University of Minnesota
- Responsible party
- Sponsor
- Investigators
- John Schmitt, Study chair, St. Catherine University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04787081
- Sponsor's protocol ID
- 938
- Status last verified
- Jan 2021
- First submitted
- 22 Jan 2021
- Last updated
- 8 Mar 2021
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Sharing plan will be determined based on researcher requests. The following could potentially be shared: blank informed consent document (attached to this registry), protocol submitted to IRB (attached to this registry), blank questionnaires and simulation observation instruments and de-identified raw numerical data from questionnaire and simulation observation instrument.
Publications
Hutson, J.A. (2020). Nighttime Postural Care Sleep-Based Outcome Measures and Education: Preparing Care Providers of Children with Cerebral Palsy (Doctoral Dissertation). University of Minnesota, Available from ProQuest Dissertations Publishing. (Dissertation Number: 27741484)
Study at a glance
From the registry record, last updated by the sponsor on 8 Mar 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Nighttime Postural Care: Caregiver Training Program and Outcome Measure Feasibility
- ClinicalTrials.gov ID
- NCT04787081
- Acronym / sponsor ID
- 938
- Conditions
- Knowledge, Attitudes, Practice
- Keywords
- competence post learning, nighttime postural care education, online caregiver education, postural care, cerebral palsy, sleep positioning
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 38 participants (actual)
- Lead sponsor
- St. Catherine UniversityUniversity, hospital or other
- Collaborators
- University of Minnesota
- Study start
- 1 Jun 2018 (actual)
- Primary completion
- 22 Sep 2018 (actual)
- Study completion
- 22 Sep 2018 (actual)
- First posted
- 8 Mar 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This experimental study investigated the feasibility of a sleep care positioning training protocol by comparing two educational interventions using a randomized control design. The overarching Population Intervention Comparison Outcomes (PICO) question was: Is the training protocol feasible for use in training caregivers? Question one includes the following sub questions: A. Is there a difference in perceived competence to implement aspects of nighttime postural care intervention or observed ability to position the person in a sleep system between caregivers receiving one training program versus another? B. Does the training protocol prepare caregivers to implement nighttime postural care (NTPC).
Detailed description
Target Population
Investigators planned to recruit a convenience sample of 40 adult participants identified as professional or non-professional care providers (primarily from two community organizations that specialize in serving clients with CP). Care providers of children (aged 6-12) with severe CP (those with limited ability to move and/or whom require use of a wheelchair) were the primary target population, since this matches the intended sample of a future intervention study. However caregivers of children outside of the 6-12 age range whom were candidates for NTPC and had similar mobility limitations as those with severe CP would not be excluded. Professional care providers could be nurses, occupational and physical therapists, assistive technology providers, etc. Non-professional care providers could be family members, care attendants, etc. Only individuals with knowledge of the child's sleep habits or routines were to be included in the study
Investigators used a mixed methods double-blind parallel group design, randomly assigning a consecutive sample of adults to an educational intervention (Lesson A or Lesson B).
Participant Recruitment
Investigators emailed flyers, recruiting participants from clinics serving persons with CP and universities educating healthcare providers and included professional and non-professional caregivers of persons with movement disorders, primarily CP with knowledge of a child's sleep habits and routines.
Participant activities
Participants completed study activities on one scheduled date: Consent process, baseline questionnaire (immediately before training), online education, post-training questionnaire, positioning of a simulated "client", post-simulation questionnaire, and exit interview. Participants completing all aspects of the study received a $50 gift card.
Randomization and blinding
The Principal Investigator (PI) enrolled participants, designating subject numbers and professional or non-professional labels. The research assistant completed randomization, drawing concealed numbers from an envelope, using Zelen's model of co-variate adaptive group randomization, and applying a threshold difference of three to balance professionals and non-professionals. An information technologist registered participants into their assigned lesson. At most five participants at a time were allowed in a classroom, with each room assigned a single lesson (A or B). Research assistants instructed participants on accessing and navigating their lesson and keeping details confidential. These processes helped ensure the PI, participants, and clinician simulation raters were not informed of lesson assignment.
Participants had the option to complete the non-assigned lesson in addition to their assigned lesson. Investigators verified participants' completion of all research activities (besides the exit interview) before the optional non-assigned lesson.
Intervention similarities and differences
Both online lessons included modules on evidence for NTPC, risk factor monitoring, sleep system types and set up, positioning methods, and outcome measures and were delivered via D2L Brightspace, a cloud-based learning management system. Both lessons' positioning-methods modules included video-based instruction. Lesson formats differed by source and design: Lesson A, created by a university's postural-care scholars using Camtasia® video creation software, consisted of interactive videos embedded with learning checkpoints, while Lesson B included written summary statements and links to freely available web-based information.
Simulation
Following their lesson and post-training questionnaire, participants positioned a "client" in a hospital bed using a designated commercial sleep system (henceforth termed "simulation"). The investigators followed protocols, instructing that participants position the client to the best of their ability, not using notes or asking observers for help; the "client" be positioned using straps to facilitate tight hamstrings in an asymmetrical-lying position common for persons with CP (i.e. head turned left, legs windswept right and knee flexed); and the clinician raters should complete the room set-up with the bed centered against the north wall, sleep system parts arranged consistently on a designated table, and that they should sit at predetermined observational locations.
Simulation raters
Health practitioners (two at a time) serving as clinician raters used the simulation observation instrument, independently observing and documenting a participant's positioning skills. An assistive technology professional and occupational therapist served as primary raters, rating 30 and 29 participants, respectively. Two secondary raters (both occupational therapists, one the PI) completed the remaining observations.
Data collection measures
Investigators collected quantitative and qualitative data using questionnaires for obtaining participants' self-perceptions of competence and lesson feedback. An observation instrument was used for scoring and describing participants' simulation performance. Fieldnotes were used for recording participant activities across the study period. The PI designed all study instruments, after reviewing competency literature, conducting a pilot study (unpublished) and consulting an academic measurement expert.
Statistical power
Before data collection, investigators chose a significance level (0.05) with plans for enrolling a minimum of 30 participants. With 15 participants per group, so there would be 80% power to detect a difference between groups of 1.06 standard deviations, where "standard deviation" describes variation within groups (i.e., Cohen's d = 1.06). Because this is the first study examining caregivers' NTPC competence from online education, no prior data could inform power calculation or supply a "standard deviation" value.
Data analysis, quantitative outcomes
Perceived Competence. Each participant provided a total average perceived competence score (total average from knowledge, ability and confidence sub-scores) at three times: baseline, post-training, and post-simulation. Investigators analyzed these scores using a mixed linear model; the random effect was participant, and fixed effects were group (Lesson A or Lesson B), professional vs. non-professional status, time (baseline, post-training, and post-simulation), and all two-way and three-way interactions. Investigators tested change over time within groups using a contrast in the group-by-time interaction (which combines professionals and non-professionals) and compared groups at each time also using contrasts in the group-by-time interaction. Statistical analyses used JMP (v. 14.0.0 Pro, SAS Institute, Cary NC).
Observed competence. Investigators computed participants' average positioning/simulation score (number correct out of 16 tasks from the simulation observation instrument) and used a mixed linear model to examine differences in observed positioning ability based on group (Lesson A or B) and professional vs. non-professional status.
Correlation of perceived and observed competence. Investigators used Pearson's correlation (r) to measure the association between participants' average self-ratings on positioning-based competence items and their average correct positioning/simulation scores, to understand the groups' ability to self-assess performance.
Interrater Reliability. Investigators measured interrater reliability using the intra-class correlation (ICC), once including all simulation observation raters and separately including the two primary clinician raters and the PI.
Data analysis, qualitative
For qualitative data, investigators used a modified grounded theory approach of open, axial and selective coding similar to that described by Bhattacherjee. From questionnaire and exit interview data, the PI read line-by-line, coding responses into categories and themes. From the simulation observation instrument, the PI listed each participant's incorrectly completed tasks and used a table to organize those tasks most frequently missed or completed incorrectly. Then clinicians' descriptive statements corresponding to incorrectly completed tasks were tabulated and reviewed line-by-line and coded into categories and themes.
Note: In addition to the above stated plan for examining the feasibility of the sleep care positioning training program, investigators also planned to examine the internal consistency reliability of the sleep disturbance scale for children (SDSC), a 27-item inventory rated on a 5 point Likert-type scale which was created by Bruni et al in 1996. To examine its reliability, study participants who self-identified as having night to night knowledge of a child with cerebral palsy's sleep performance were asked to complete the SDSC. While data was collected for this aspect of the study, only 10 participants self-identified as having such knowledge; thus, further analysis of the tools' reliability was not completed by investigators.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Mixed methods double-blind parallel group design, involving a consecutive sample of adults being randomly assigned to an educational intervention (Group A or B). The Principal Investigator enrolled participants, designating subject numbers and professional or non-professional labels. The research assistant completed randomization, drawing concealed numbers from an envelope to determine participant's educational intervention group (A or B). To balance the number of professionals and non-professionals across groups, the research assistant used co-variate adaptive group randomization and applied a difference threshold of 3.
| Arm | Type | Receives |
|---|---|---|
| Sleep Care Positioning Training Program GRP1 | Experimental | Other: Sleep Care Positioning Training Program GRP1A sleep care positioning lesson created by a University's postural-care scholars using Camtasia® video creation software with modules on evidence for night-time postural care, risk factor monitoring, sleep system types and set up, positioning methods, and outcome measures. This lesson consisted of interactive videos embedded with learning checkpoints. All videos included narration and closed captioning. The following link contains the videos which were modified post-study to reflect some of the participant's feedback: https://stkatentpc.weebly.com/ |
| Sleep Care Positioning Training Program GRP2 | Active comparator | Other: Sleep Care Positioning Training Program GRP2A sleep care positioning lesson created by a research assistant along with the principal investigator with modules on evidence for night-time postural care, risk factor monitoring, sleep system types and set up, positioning methods, and outcome measures. This lesson consisted of primarily written summary statements and links to freely available web-based information. Most of this lesson's modules included written information that the participant would need to read with the exception of the positioning methods modules. For the positioning module, participants were provided with links to manufacturers' websites which contained video clips on how to place postural supports. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Professional and non-professional caregivers of children with movement disorders or cerebral palsy.
Key exclusion criteria (1 listed)
- Caregivers without knowledge of sleep habits and routines of persons with such diagnoses
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Sleep Care Positioning Training Program GRP1Also: Lesson AVideo-based tutorial covering six nighttime postural care topic areas which contained narration and closed captioning. This 2-hour online training program was delivered in a University classroom via D2L Brightspace. | Other | Sleep Care Positioning Training Program GRP1 |
| Sleep Care Positioning Training Program GRP2Also: Lesson BWeb-link based tutorial covering six nighttime postural care topic areas which contained mostly written content. This self-paced online training program was delivered in a University classroom via D2L Brightspace. | Other | Sleep Care Positioning Training Program GRP2 |
Primary outcome
Baseline Sleep Care Positioning Questionnaire
Time frame: Completed immediately before training/educational intervention. Same day as training.
Perceived competence questionnaire with 4-pt. ratings of knowledge, ability and confidence for nighttime postural care research, risk factor monitoring, sleep system types / set-up, positioning a person, and measuring outcomes.
Post Sleep Care Positioning Program Questionnaire
Time frame: Completed immediately after training / educational intervention. Same day as training.
Perceived competence questionnaire with 4-pt. ratings of knowledge, ability and confidence for nighttime postural care research, risk factor monitoring, sleep system types / set-up, positioning a person, and measuring outcomes.
Post Simulation Sleep Care Positioning Program Questionnaire
Time frame: Completed immediately after simulation activity, after positioning a person in a sleep system. Same day as training.
Perceived competence questionnaire with 4-pt. ratings of knowledge, ability and confidence for nighttime postural care research, risk factor monitoring, sleep system types / set-up, positioning a person, and measuring outcomes.
1 secondary outcome
Simulation Observation Instrument
Time frame: Completed after training and post-training questionnaire. Same day as training.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Mar 2021.
- BackgroundHutson, J.A. (2020). Nighttime Postural Care Sleep-Based Outcome Measures and Education: Preparing Care Providers of Children with Cerebral Palsy (Doctoral Dissertation). University of Minnesota, Available from ProQuest Dissertations Publishing. (Dissertation Number: 27741484)
- The sleep care positioning training program (Lesson A) which was provided to Group 1. The version found at this site contains some edits based on the feedback provided by participants during the research study.Link provided by the sponsor.
- Jennifer Hutson's dissertation which contains a detailed description of the study and its outcomes (information about this study is primarily contained within chapters 3 \& 4 of the dissertation).Link provided by the sponsor.
- Individual participant dataSharing planned: Yes. Sharing plan will be determined based on researcher requests. The following could potentially be shared: blank informed consent document (attached to this registry), protocol submitted to IRB (attached to this registry), blank questionnaires and simulation observation instruments and de-identified raw numerical data from questionnaire and simulation observation instrument.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
John Schmitt study chair
St. Catherine University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Sleep Care Positioning Training Program GRP1 and Sleep Care Positioning Training Program GRP2 in people with Knowledge, Attitudes, Practice, run by St. Catherine University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 8 Mar 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Baseline Sleep Care Positioning Questionnaire (time frame: Completed immediately before training/educational intervention. Same day as training.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04787081, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Mar 2021.