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Implementation and evaluation of two different cognitive stimulation therapy training approaches

An evaluation and comparison of the effectiveness of two different cognitive stimulation therapy (CST) approaches and their implementation in practice

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN28793457
Enrollment
240
Registered
2011-03-10
Start date
2011-02-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Dementia Mental and Behavioural Disorders Dementia

Interventions

Randomised controlled trial (RCT): In the RCT all staff members will be expected to attend training and will receive two manuals, workbook and DVD. They will then be randomised to rece

Sponsors

North East London NHS Foundation Trust (NELFT) (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Staff: 1. Staff members' working directly for people with dementia 2. Willingness to self complete three sets of questionnaires within a year time frame 3. Adequate written and spoken comprehension of the English language 4. Opportunity to recruit five to eight suitable people in the mild to moderate stages of dementia 5. Access to a computer and an adequate level of competency to complete questionnaires online 6. Each centre will contribute three or more staff members who will intend to run CST groups 7. Agreement with management to have two hours, set aside, each week to run CST sessions and one hour a week, set aside, for the following 24 weeks of maintenance CST groups Person with dementia: 1. Previous diagnosis of mild to moderate dementia, with a score of between 0.5 and 2 on the Clinical Dementia Rating 2. Adequate spoken and written English 3. Ability to participate in a 'meaningful' conversation 4. Good eyesight and hearing 5. Level of comprehension to willingly give informed consent to take part in groups 6. Ability to partake in a group for 45 minutes 7. Willingness to complete the QoL-AD and Mini-Mental State Examination (MMSE) at three intervals over a year time frame 8. Do not have a major physical illness or disability which could affect participation 9. Do not have a diagnosis of a learning disability Both: 10. Male and female, aged between 18 - 99 years

Exclusion criteria

Exclusion criteria: Staff: 1. Not having direct access to people with dementia 2. Not being able to recruit between five to eight people with dementia 3. Unable to complete self-completing questionnaires 4. Inability to access or use a computer 5. Unable to write or speak fluently in English 6. Inability to provide three staff members to take part in the the trial 7. No consent from management Person with dementia: 1. No diagnosis of dementia 2. Inability to write or speak fluently in English 3. Unable to enagage in a conversation 4. Unable to stay in a group for 45 minutes 5. Bad eyesight or hearing 6. Unable to give informed consent 7. Not willing to complete minimal outcome measures

Design outcomes

Primary

MeasureTime frame
1. Number of attendees to the CST groups 2. Level of adherence 3. Competency of staff member For staff the measures will be completed at baseline, 6 and 12 months. For the people with dementia they will be measured at baseline, 7 and 31 weeks.

Secondary

MeasureTime frame
1. Minimal outcome measures with person with dementia (cognition and quality of life) 2. Job satisfaction 3. Approaches to dementia 4. Dementia knowledge 5. Learning transfer system inventory 6. Barriers to change For staff the measures will be completed at baseline, 6 and 12 months. For the people with dementia they will be measured at baseline, 7 and 31 weeks.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 26, 2026