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Trial of a Medical and Mental Health Unit for Older People (TEAM)

Primary Purpose

Dementia, Confusion, Cognitive Impairment

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
A medical and mental health unit
Sponsored by
University of Nottingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Dementia focused on measuring Mental Health, Aged, Hospitals, general, Dementia, Delirium, Dementia and confusion

Eligibility Criteria

65 Years - 120 Years (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient participants will be over 65, admitted as an emergency to Nottingham University Hospital NHS Trust, with an established or possible physical health problem and concurrent 'confusion', clinically eligible for management on the Medical and Mental Health Unit.
  • Carer participants will be a family member or carer, in regular contact with the patient participant, to serve both as an informant, and, and to study carer health and outcomes.
  • Confusion will be loosely defined, including working diagnoses of:
  • Delirium
  • Dementia
  • Dementia with a suspicion of super-added delirium

Exclusion Criteria:

  • Those who require sectioning under the Mental Health Act
  • Those with intoxication to illicit drugs or alcohol, or the immediate care of patients with overdose
  • Those with a primary psychiatric problem in the absence of suspected significant physical or functional co-morbidity.
  • Those who are severely medically ill, requiring intensive monitoring or therapy (critical care), or sub-specialist medical intervention (e.g. severe acute GI bleeding, respiratory support).
  • Those with an overriding clinical need for management in another service e.g. stroke, orthogeriatric, renal, oncology.
  • Those with personality disorder, depression or anxiety as the primary psychiatric diagnosis.
  • Those who are registered with a non - Nottingham Primary Care Trust General Practitioner.
  • Those who do not speak English and have no family translator.

Sites / Locations

  • Nottingham University Hospitals NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

A Medical and Mental Health Unit

Standard care wards

Arm Description

A specialist unit for cognitively impaired older patients admitted as a medical emergency to the acute hospital.

The standard care provided by the acute hospital for cognitively impaired older patients admitted as a medical emergency.

Outcomes

Primary Outcome Measures

Number of days at home in the 3 months after randomisation
The primary outcome will be number of days spent at home in the three months following recruitment (or remaining in a care home for those previously resident at recruitment). This encompasses mortality, discharge, length of hospital stay, and ability to sustain discharge and avoid readmission. 'Days at home' will be calculated as 90 days minus the nuimber of days spent dead, in residential intermediate care units, in hospital, in respite care or in a new care home placement at a higher level of dependency.

Secondary Outcome Measures

Quality of life
Dementia quality of life (Demqol, patient and proxy) and generic quality of life (Euroqol EQ5D).
Behavioural disability
Neuropsychiatric inventory.
Mortality
Personal activities of daily living
Barthel ADL Index
Participant / generic disability
short London Handicap Scale
Cognition
MMSE, in particular to detect recovery of delirium
Carer satisfaction with hospital care
Satisfaction with care received questionnaire
Carer strain and general health
Carer strain index and carer general health questionnaire GHQ-12.
Service Outcomes
Days in each type of ward. Hospital re-admissions, and total hospital length of stay. New institutionalisation (or moving to a higher level of dependency for those in a care home) Days in a care home (including respite care) GP visits, and use of other primary care contacts (district nurse, community matron, practice nurse) Hospital appointments Attendances at physical and mental health day hospitals Contact with community mental health teams (including community psychiatric nursing) Use of ambulance service Use of social service home care and day centres.
Quality of care and patient experience on the ward
Quality of care and patient experience will be measured using Dementia Care Mapping on both the MMHU and standard care. Dementia Care Mapping provides a structured record of activity levels, mood and engagement of participants and the quality of staff interactions over a 4-6 hour period.
Health and social care costs
Service outcomes will be costed using specific costs where available or standard reference costs otherwise.

Full Information

First Posted
June 2, 2010
Last Updated
December 1, 2015
Sponsor
University of Nottingham
Collaborators
National Institute for Health Research, United Kingdom, Nottingham University Hospitals NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT01136148
Brief Title
Trial of a Medical and Mental Health Unit for Older People
Acronym
TEAM
Official Title
Evaluation of a Medical and Mental Health Unit Compared With Standard Care for Older People Whose Emergency Admission to an Acute General Hospital is Complicated by Concurrent 'Confusion'.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nottingham
Collaborators
National Institute for Health Research, United Kingdom, Nottingham University Hospitals NHS Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This research is an evaluation of the MMHU compared to standard care. Patients who are over 65 and 'confused' at admission will be randomly allocated to the MMHU or standard care. The MMHU does not have capacity for all confused older patients admitted to NUH, and random allocation is similar to what happens in practice currently. For this study, 480 of these patients will be recruited, together with a carer (240 from the MMHU, 240 from standard care wards). The investigators will collect baseline information about the patient participant's physical and mental health and disability. The investigators will count the total days spent at home and measure patient participants' health status after 3 months, and use of resources over six months. Carer strain and quality of life will be measured at baseline and follow up.
Detailed Description
The objectives of this study are: To evaluate whether a specialist multidisciplinary MMHU for older people with 'confusion', admitted to a general hospital as an emergency, is associated with better outcomes than standard care. To study the quality of care on the MMHU compared with standard care To perform a health economic analysis, from the perspective of health and social care. The principal hypotheses being tested are: That care on the MMHU is associated with more days spent at home (in the 3 months after recruitment) than care on standard wards That care on the MMHU is associated with better health status measured at 3 months, in terms of quality of life, behavioural disturbance, cognitive function, disability, participation, mortality and care home residence. That care on the MMHU is associated with better psychological well being amongst carers and reduced carer strain compared with standard care. That the quality of care and patient experience for patients on the MMHU is superior to that on standard care wards. That care on the MMHU is cost-effective compared with that on standard care wards. The setting for the study is a large NHS acute teaching hospital organisation with 2 campuses (Queens Medical Centre and City Hospital), comprising 1800 beds, serving a population of 700 000 for general hospital services. Sample size is determined by available resources. 240 patients randomised to the MMHU unit over 24 months, and an equal number of controls, should be sufficient to measure, with 80% power, a 3 to 6-day reduction in length of stay, and 15% increase in the proportion of participants discharged home (e.g. 50% to 65%). Power will be greater for scaled outcomes, and the 'days at home' outcome. The main study will run for up to 24 months from July 2010. Follow up will be 3 months after randomisation. Prior to trial commencement we will run 1 or 2 short pilot studies, during which we will test the recruitment and ward allocation processes. The study is designed to be robust, despite being constrained by the operational needs of the clinical service, and both service and research capacity. The NHS Trust clinical service has agreed that, for the duration of the study, allocation to the MMHU will be by randomisation. This is not part of the research, but represents clinical service support for it. Potential participants will be identified by the Acute Medical Unit, on simple criteria (''confused', over 65'). The MMHU will confirm clinical eligibility and complete a screening log. If there is a bed available on MMHU the patient will be randomised using an internet based randomisation system (with stratification on care home residence), and the patient assigned to MMHU or a standard care ward. Non-randomised patients can be referred, and, if appropriate, randomised, later in their hospital stay. Research eligible patients and carers will be invited to participate in research, once on their allocated ward. Consent and participation will be for data collection, observation of care, and follow up only. Excluded patients will continue on their allocated ward outside the trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia, Confusion, Cognitive Impairment, Delirium
Keywords
Mental Health, Aged, Hospitals, general, Dementia, Delirium, Dementia and confusion

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
600 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A Medical and Mental Health Unit
Arm Type
Experimental
Arm Description
A specialist unit for cognitively impaired older patients admitted as a medical emergency to the acute hospital.
Arm Title
Standard care wards
Arm Type
Active Comparator
Arm Description
The standard care provided by the acute hospital for cognitively impaired older patients admitted as a medical emergency.
Intervention Type
Behavioral
Intervention Name(s)
A medical and mental health unit
Intervention Description
A specialist medical and mental health unit with both physician and psychiatric medical and nursing staff, and mental health experienced therapists. Emphasis will be on early and accurate diagnosis, multidisciplinary management, rigorous communication and goal setting, discharge planning and interface with community services.
Primary Outcome Measure Information:
Title
Number of days at home in the 3 months after randomisation
Description
The primary outcome will be number of days spent at home in the three months following recruitment (or remaining in a care home for those previously resident at recruitment). This encompasses mortality, discharge, length of hospital stay, and ability to sustain discharge and avoid readmission. 'Days at home' will be calculated as 90 days minus the nuimber of days spent dead, in residential intermediate care units, in hospital, in respite care or in a new care home placement at a higher level of dependency.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Quality of life
Description
Dementia quality of life (Demqol, patient and proxy) and generic quality of life (Euroqol EQ5D).
Time Frame
3 months
Title
Behavioural disability
Description
Neuropsychiatric inventory.
Time Frame
3 months
Title
Mortality
Time Frame
3 month
Title
Personal activities of daily living
Description
Barthel ADL Index
Time Frame
3 months
Title
Participant / generic disability
Description
short London Handicap Scale
Time Frame
3 months
Title
Cognition
Description
MMSE, in particular to detect recovery of delirium
Time Frame
3 months
Title
Carer satisfaction with hospital care
Description
Satisfaction with care received questionnaire
Time Frame
1-3 weeks post discharge from index admission
Title
Carer strain and general health
Description
Carer strain index and carer general health questionnaire GHQ-12.
Time Frame
3 months
Title
Service Outcomes
Description
Days in each type of ward. Hospital re-admissions, and total hospital length of stay. New institutionalisation (or moving to a higher level of dependency for those in a care home) Days in a care home (including respite care) GP visits, and use of other primary care contacts (district nurse, community matron, practice nurse) Hospital appointments Attendances at physical and mental health day hospitals Contact with community mental health teams (including community psychiatric nursing) Use of ambulance service Use of social service home care and day centres.
Time Frame
3 months
Title
Quality of care and patient experience on the ward
Description
Quality of care and patient experience will be measured using Dementia Care Mapping on both the MMHU and standard care. Dementia Care Mapping provides a structured record of activity levels, mood and engagement of participants and the quality of staff interactions over a 4-6 hour period.
Time Frame
During hospital stay.
Title
Health and social care costs
Description
Service outcomes will be costed using specific costs where available or standard reference costs otherwise.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
120 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient participants will be over 65, admitted as an emergency to Nottingham University Hospital NHS Trust, with an established or possible physical health problem and concurrent 'confusion', clinically eligible for management on the Medical and Mental Health Unit. Carer participants will be a family member or carer, in regular contact with the patient participant, to serve both as an informant, and, and to study carer health and outcomes. Confusion will be loosely defined, including working diagnoses of: Delirium Dementia Dementia with a suspicion of super-added delirium Exclusion Criteria: Those who require sectioning under the Mental Health Act Those with intoxication to illicit drugs or alcohol, or the immediate care of patients with overdose Those with a primary psychiatric problem in the absence of suspected significant physical or functional co-morbidity. Those who are severely medically ill, requiring intensive monitoring or therapy (critical care), or sub-specialist medical intervention (e.g. severe acute GI bleeding, respiratory support). Those with an overriding clinical need for management in another service e.g. stroke, orthogeriatric, renal, oncology. Those with personality disorder, depression or anxiety as the primary psychiatric diagnosis. Those who are registered with a non - Nottingham Primary Care Trust General Practitioner. Those who do not speak English and have no family translator.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John R Gladman
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nottingham University Hospitals NHS Trust
City
Nottingham
ZIP/Postal Code
NG7 2UH
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
26684872
Citation
Tanajewski L, Franklin M, Gkountouras G, Berdunov V, Harwood RH, Goldberg SE, Bradshaw LE, Gladman JR, Elliott RA. Economic Evaluation of a General Hospital Unit for Older People with Delirium and Dementia (TEAM Randomised Controlled Trial). PLoS One. 2015 Dec 18;10(12):e0140662. doi: 10.1371/journal.pone.0140662. eCollection 2015.
Results Reference
derived
PubMed Identifier
24613652
Citation
Goldberg SE, Whittamore KH, Pollock K, Harwood RH, Gladman JR. Caring for cognitively impaired older patients in the general hospital: a qualitative analysis of similarities and differences between a specialist Medical and Mental Health Unit and standard care wards. Int J Nurs Stud. 2014 Oct;51(10):1332-43. doi: 10.1016/j.ijnurstu.2014.02.002. Epub 2014 Feb 15.
Results Reference
derived
PubMed Identifier
23819964
Citation
Goldberg SE, Bradshaw LE, Kearney FC, Russell C, Whittamore KH, Foster PE, Mamza J, Gladman JR, Jones RG, Lewis SA, Porock D, Harwood RH; Medical Crises in Older People Study Group. Care in specialist medical and mental health unit compared with standard care for older people with cognitive impairment admitted to general hospital: randomised controlled trial (NIHR TEAM trial). BMJ. 2013 Jul 2;347:f4132. doi: 10.1136/bmj.f4132.
Results Reference
derived
PubMed Identifier
21569471
Citation
Harwood RH, Goldberg SE, Whittamore KH, Russell C, Gladman JR, Jones RG, Porock D, Lewis SA, Bradshaw LE, Elliot RA; Medical Crises in Older People Study Group (MCOP). Evaluation of a Medical and Mental Health Unit compared with standard care for older people whose emergency admission to an acute general hospital is complicated by concurrent 'confusion': a controlled clinical trial. Acronym: TEAM: Trial of an Elderly Acute care Medical and mental health unit. Trials. 2011 May 13;12:123. doi: 10.1186/1745-6215-12-123.
Results Reference
derived

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Trial of a Medical and Mental Health Unit for Older People

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