Improving Staff Attitudes and Care for People With Dementia: eLearning (tEACH)

September 25, 2018 updated by: King's College London

An eLearning Optimized Person Centred Intervention to Improve Staff Attitudes and Quality of Care for People With Dementia Living in Care Homes

The primary objective of this study is to determine whether a Person Centred Care online training programme confers significant benefit in terms of improving staff attitudes and quality of care of residents with dementia living in care homes, in comparison to enhanced usual training for professional care staff.

There is considerable interest in e-learning and dementia from care home providers. Significant investment has been made into the production of resources for care staff but to date there appears to be no, or very limited, evaluation of their effectiveness.

The aim is to provide a cost-effective, simple and practical evidence-based intervention, improving staff attitudes towards residents with dementia and quality of care provision. The trial will be a randomized controlled 3-arm cluster single blind trial that will take place over 9 months in 24 care homes in the UK.

Study Overview

Detailed Description

The National Institute for Health Research (NIHR) funded Well-being and Health for People with Dementia (WHELD) programme, An Optimized Person Centred Intervention to Improve Quality of Life for People with Dementia Living in Care Homes. This optimized intervention is based on a factorial study and qualitative evaluation, to combine: training on person-centred care, promoting person-centred activities and interactions, and providing care home staff and general practitioners with updated knowledge regarding optimal use of psychotropic medications for persons with dementia in care homes. Using a train-the-trainer model, the intervention was delivered by trained therapists, who trained 2 lead care staff members (WHELD champions) within each care home to implement the intervention over a 9-month period.

The primary objective of this study involving 24 care homes, with approximately 240 care staff, is to determine whether an online version of the optimized WHELD intervention, with or without supervision support, confers significant benefit in terms of improving attitudes of care staff caring for people with dementia and quality of care of residents with dementia living in care homes.

There is considerable interest in e-learning and dementia. Significant investment has been made into the production of resources for care staff but to date there appears to be no, or very limited, evaluation of the effectiveness of e-learning in either raising awareness amongst care staff, or increasing outcomes of care for people with dementia. In spite of the lack of evidence, e-learning remains popular with care home providers and managers, as they are perceived to be low-cost, can be delivered to staff on-site or even at home, and with minimal disruption to staffing routines and schedules.

The e-learning programme is based on the aforementioned WHELD RCT programme, which included over 80 care homes and 1000 participants in the study, and has already shown significant benefits in improvements in quality of life and agitation. This study will provide pilot testing to evaluate the effectiveness of an e-learning version.

Key secondary objectives will be to determine the specific impact of the e-learning intervention on a range of outcomes including quality of care, quality of the interaction of care staff with people with dementia, person-centered practice, staff knowledge about dementia and staff general health, work stress and experience working with residents with dementia.

The investigators hypothesize that the intervention (in particular with supervision support) will significantly improve several key outcomes. Specifically, the investigators hypothesize that, compared to enhanced usual training, the optimized e-learning intervention will:

• Improve staff attitudes towards people with dementia

The secondary hypotheses are that the WHELD e-learning intervention will:

  • Improve quality of care
  • Improve quality of interactions between staff and residents
  • Improve person-centred practice
  • Increase staff knowledge about dementia
  • Improve staff general health
  • Reduce staff work stress
  • Improve satisfaction in caring for people with dementia

Baseline, post intervention and 4-month follow up data will be collected on all consented participants who meet the inclusion criteria at each participating care home.

Study Type

Interventional

Enrollment (Actual)

282

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • London, United Kingdom, SE1 1UL
        • King's College London

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Care Home Selection:

Inclusion Criteria:

  • Care homes that have residential or nursing status and are registered to provide care for people with dementia.
  • Care homes randomly selected from the Care Home Research Network
  • Research enabled and actively engaged in ENRICH programme
  • Care homes should be able to demonstrate an acceptable standard of care according to Care Quality Commission (CQC).
  • Prepared to release staff to complete training and to implement interventions
  • Have a manager in post who is willing/able to act as key link person for trial
  • "Tech ready" home - staff have access to PCs or tablets in the care home

Exclusion criteria:

  • Less than 60% of the residents have dementia
  • Care home is receiving special support from their local authority
  • Care home has failed to meet more than 1 of the 5 CQC care home quality standards checks
  • Insufficient staffing resource: Care home unable to provide care staff for training

Participant Selection:

Inclusion Criteria:

  • Sufficient competence in English to undertake the training programme
  • Qualified and unqualified paid care staff
  • Permanent or contract employees providing direct care to residents
  • Has basic computer literacy

Exclusion Criteria:

• Bank or agency staff

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Arm 1: Regular Contact Group (WHELD +)
Regular Contact Group (WHELD elearning package + regular supervision support) A research associate will provide one face-to-face training session with participating care staff in the care home on how to use the online modules, providing a walk-through demonstration to ensure all are comfortable with the programme and its technology. The research associate will provide light touch support by returning fortnightly throughout the intervention period to the care home to observe/troubleshoot around online programme.
The e-learning WHELD intervention The optimised e-learning programme will consist of five 25-minute interactive online modules based on a recently completed RCT of an in person training programme (WHELD), combining the most effective elements of existing approaches to create a comprehensive but practical staff training intervention. Based on a factorial study and qualitative evaluation, WHELD combines: person-centred care, person-centred activities and interactions, and updated knowledge regarding optimal use of psychotropic medications.
Experimental: Arm 2: Online Contact Group (WHELD only)
Online Contact Group (WHELD elearning package only) The e-learning modules will be emailed to the care home with clearly written instructions on how to access the course.
The e-learning WHELD intervention The optimised e-learning programme will consist of five 25-minute interactive online modules based on a recently completed RCT of an in person training programme (WHELD), combining the most effective elements of existing approaches to create a comprehensive but practical staff training intervention. Based on a factorial study and qualitative evaluation, WHELD combines: person-centred care, person-centred activities and interactions, and updated knowledge regarding optimal use of psychotropic medications.
No Intervention: Arm 3: Enhanced usual practice Control Group

Arm 3: Enhanced usual practice Control Group (with information/signposting re high quality on line e-learning and educational materials).

This will consist of a 2-page written guidance sheet on the best freely available dementia e-learning programmes and a one-off meeting with a research associate in the care home to explain the information/signposting

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Approaches to Dementia Questionnaire (ADQ) assessing change between time points
Time Frame: T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
This measure includes 19 attitudinal items, each scored from 1 (strongly disagree) to 5 (strongly agree) [3]. They are summed to form a total score (range 19-95) as well as a hope subscore (8 items, range 8-40) and a person-centred subscore (11 items, range 11-55). Higher scores indicate more positive attitudes. Example items indicative of hope (reverse scored) include ''people with dementia are very much like children'' and ''it is important not to become too attached to residents.'' Items related to person-centred care include ''it is important for people with dementia to be given as much choice as possible in their daily lives'' and ''people with dementia need to feel respected, just like anybody else.''
T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dementia Care Mapping assessing change between time points
Time Frame: T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
This measure will be used as an observation tool to assess quality of care [4]. DCM is an established and National Institute for Clinical Excellence/Social Care Institute for Excellence (NICE/SCIE) recommended, routine care home/NHS practice development intervention that is regularly used for ensuring a systematic approach to providing individualised person-centred care. It is used to support the sustained implementation of PCCT in dementia care practice. DCM is an observational tool, set within a practice development cycle. There is good evidence of its use in practice settings as a quality audit and improvement tool.
T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
The General Health Questionnaire-12 assessing change between time points
Time Frame: T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
This measure is a widely used short screening instrument comprised of 12 items [5]. Goldberg and colleagues (1997) found the GHQ-12 to have good overall sensitivity (83.4%) and specificity (76.3%). The mean area under the ROC curves was 0.88 with a narrow range. Goldberg and colleagues (1997) scored the scales using both the GHQ method (0-0-1-1) as well as using a Likert method (0-1-2-3). It was found, for the GHQ-12, that the GHQ method was better for specificity and sensitivity than the Likert method. The GHQ-12's validity characteristics were not significantly different when accounting for gender, age group or educational level.
T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
Staff Experience Working with Residents with Dementia assessing change between time points
Time Frame: T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
This measure includes 21 items assessing satisfaction, each scored from 0 (not at all) to 4 (extremely) and summed to create a total score ranging from 0 to 84 [6]. Higher scores indicate more satisfaction, and subscales can be created for each of six domains: (satisfaction with) feedback, the care organization, one's own expectations, patient contact, expectations of others, and the environment.
T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
Knowledge in Dementia Scale assessing change between time points
Time Frame: T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
This measure is a 16-item self-report questionnaire used to measure knowledge in dementia [7]. The questionnaire is scored on an agree/disagree scale; 'agree' responses are given a score of 1, 'disagree' responses are given a score on 0. This means that it is possible to gain a total score between 0 and 16, a higher score being representative of better knowledge about dementia.
T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
Quality of Interactions Schedule assessing change between time points
Time Frame: T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
This measure is an observational tool that measures the quality of interactions between staff and resident and person-centred environment in care home settings [8].
T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
Inventory of Geriatric Nursing Self-Efficacy assessing change between time points
Time Frame: T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up
This measure is a 9-item measure specifically developed for individuals providing nursing care to geriatric populations to quantify the extent to which individuals perceive themselves able to manage common sources of caregiver stress
T1: baseline, T2: up to 2 weeks post intervention, T3: 4 month follow up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Professor Clive Ballard, King's College London

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2016

Primary Completion (Actual)

May 7, 2017

Study Completion (Actual)

July 1, 2018

Study Registration Dates

First Submitted

June 29, 2017

First Submitted That Met QC Criteria

July 3, 2017

First Posted (Actual)

July 5, 2017

Study Record Updates

Last Update Posted (Actual)

September 26, 2018

Last Update Submitted That Met QC Criteria

September 25, 2018

Last Verified

September 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 196661 16/WA/0090 tEACH

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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