Multiple Sclerosis Clinical Trial
Official title:
An Exploratory Randomized Controlled Trial of a Manualized, Nurse-led, Telephone Intervention Support Service for Support Persons of People With Multiple Sclerosis
The primary aim of this study is to determine if a manual based telephone intervention support service for people who support people with Multiple Sclerosis (PwMS), initiated by nurse specialists who provide care to PwMS, has a positive impact on the lives of PwMS and their support persons. For support persons this impact is determined by measurable support person/carer self-efficacy and preparedness to care, burden, quality of life, service utilization and satisfaction with the support service. For PwMS this is determined by their qualitative experience of the type of care they receive from their carer. A secondary aim is to determine the possible economic benefits of the introduction of such an intervention nationally. A support person is the person nominated by the PwMS as the person who provides the most support or physical assistance to a person with MS who is not a paid service provider.
The negative impact of caregiving on caregivers of People with Multiple Sclerosis (PwMS) has
been well documented (Corry & While, 2008). Outside of scheduled health care contacts,
caregivers usually make contact with nurse specialists when in distress or in crisis
situations. Nurses specialising in MS have specialised knowledge in caring for PwMS and
their caregivers and the management of symptoms of MS, and are well positioned to provide
specialist advice, information and referral. Much of the unique support given to caregivers
of PwMS by MS nurses in Ireland is undocumented so that their impact upon patient and carer
outcomes is unknown.
The well-being of caregivers of PwMS is crucial with limited budgets resulting in increased
reliance upon caregivers to provide ongoing support for PwMS. Health care professionals need
to prioritise health promotion, information giving and pro-active management of situations
among caregivers of PwMS if the deleterious effects of care-giving on the PwMS and their
caregivers are to be minimised and poor health avoided.
A search of the literature revealed that no published studies exist on the use of telephone
support interventions for caregivers of PwMS. The extent to which telephone support
interventions have been used in an attempt to support caregivers is evident from the number
of studies found on carer telephone support across a number of illnesses (n=29). The range
of care recipients, research designs and objectives for the studies make it difficult to
draw definitive conclusions regarding particular outcomes and interventions. However,
positive findings include feeling supported (Bank et al. 2006, Stewart et al. 2001), feeling
empowered (Wilkes et al. 2004; Stewart et al. 2001) and reduced carer burden (Bormann et al.
2009; Tremont et al. 2008; Stewart et al. 2001).
The positive findings from the studies on telephone support interventions, along with the
current use of carer telephone contact with NSMS when in crisis, suggest that a nurse
specialist proactive approach to problem management, information and advice giving has
potential for positive outcomes for caregivers of PwMS.
For the purpose of this study a carer is defined as a person who provides the most support
or physical assistance to a PwMS, and who is not a paid service provider.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
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