Improving Monitoring of Patients Receiving Case Management
NCT ID: NCT01597882
Last Updated: 2014-02-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
114 participants
OBSERVATIONAL
2012-10-31
2013-12-31
Brief Summary
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One approach to help patients with long term conditions is case management, where by (usually) a community matron visits patients at home, looking for early warning signs of any worsening of their condition and arranging care and treatment. But the current way this is done varies across the country and hospital admissions are still rising. In order to give the right care at the right time, effective monitoring is needed to help the community matron detect and act on changes in the patient's condition.
Loss of muscle strength in old age is linked to a poor health, but it is not known whether simple measures of muscle strength could be used to detect and predict declines in health in the short to medium term to help maintain independence and prevent an accident or hospital admission.
The aim of this study is to look at whether monitoring muscle strength in case managed patients is practical, acceptable and useful in detecting when a patient's condition worsens. Each patient will be visited by the researcher in their home twice in the first week, then once every two weeks, for another 5 weeks, to carry out three simple measures of grip and respiratory strength, and complete questionnaires about their health and ability to carry out day to day activities. Each visit will last about 20 to 30 minutes. A small group of clinicians will be asked about their views of the strength measures. Database analysis will allow descriptive data on the patient group to be gathered and analysed.
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Detailed Description
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Conditions
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Study Design
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COHORT
Study Groups
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Case managed patients
Patients aged 65 years and over receiving community case management.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
2. Preclude consent:
* Significant cognitive impairment resulting in lack of capacity to consent. b. Unable to communicate without significant aids e.g. Non-English speaking.
3. Preclude participation/ collection of data
* Significant emotional distress or psychotic illness active within the last 6 months.
* Receiving end of life care.
* Current illness that would preclude data collection.
* Upper limb pathology that would limit participation e.g. bone fracture within the previous 6 months.
* Identified as high risk patients with regards to lone working safety by their case manager.
65 Years
ALL
No
Sponsors
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University of Southampton
OTHER
Responsible Party
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Nicola Barnes
Post-graduate Research Student
Principal Investigators
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Nicola Barnes, MPharm
Role: PRINCIPAL_INVESTIGATOR
University of Southampton
Locations
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Solent NHS Trust
Portsmouth, , United Kingdom
Southern Health NHS Foundation Trust
Southampton, , United Kingdom
Countries
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Other Identifiers
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1409-ERGO
Identifier Type: OTHER
Identifier Source: secondary_id
8550
Identifier Type: -
Identifier Source: org_study_id
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