An evaluation of an online mindfulness programme for people with multi
Comparing the clinical- and cost-effectiveness of an internet-delivered mindfulness-based program with waitlist controls among adults with progressive MS
What it found
We found no results in the registry or in papers.
This trial finished 7 years ago. We found no results in the registry or in any paper that cites it.
What it measured
Main measures
General levels of distress are measured using the 12-item General Health Questionnaire (GHQ-12) at 3 time points such as week immediately pre intervention, during the week post intervention and at 3 month follow up
Other measures (1)
1. Severity of current symptoms of depressive disorders are measured using the Beck Depression Inventory (BDI) 3 time points such as week immediately pre intervention, during the week post intervention and at 3 month follow up 2. Pain severity and the degree of interference with function is measured using the Beck Pain Inventory short form (BPI-SF) at 3 time points such as week immediately pre int
FatiguePainMood and sleepQuality of life (reported by participants)
Who could take part
Progressive MS · 18 and over
Show the full criteria
Inclusion criteria
Inclusion: 1. Aged 18 years or more 2. Diagnosis of primary or secondary progressive MS 3. Internet access 4. Not currently undergoing any form of psychological treatment 5. First language English 6. Resident in Ireland, not currently experiencing a psychotic illness and/or cognitive impairment. Exclusion: 1. Participants undergoing any form of psychological treatment 2. Participants experiencing a psychotic illness and/or cognitive impairment 3. Participation in any other form of psychological intervention in addition to the study intervention is prohibited during the trial
Exclusion criteria
Not separately supplied in the registry.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
IBackground and study aims Multiple Sclerosis (MS) is a lifelong disease of the nervous system (i.e. the brain, spinal cord and optic nerves). Symptoms can vary from mild sensational problems such as tingling to severe disability. The cause is currently unknown and there is no cure. MS typically develops between the ages of 20 and 40 and is twice as common in women as men. Approximately 2.3 million people worldwide have a diagnosis of MS. MS is typically diagnosed in young to mid-adulthood, at which age, family and career are very important. Potential disruptions to social relationships due to mobility issues, sexual dysfunction and financial problems following employment issues can further impact on emotional wellbeing in people with MS. It is therefore not surprising that people with MS report feeling depressed, anxious, distressed, tired and in pain. Thus, the psychological well-being of people living with MS is also of great importance. Research indicates that mindfulness interventions have been found to alleviate MS-related symptoms. Mindfulness has been defined as ‘paying attention, in a particular way; on purpose, in the present moment and non-judgmentally’ and thus, can encourage more positive coping responses. The aim of this research is to develop an online mindfulness programme for people living with MS. Who can participate? Adults aged 18 and older who are diagnosed with MS. What does the study involve? Participants are randomly allocated to one of two groups. Those in the first group receive the MindfulnessforMS programme which consists of eight weekly sessions. Participants are contacted in order to be motivated to continue with the programme. Those in the second group are on a waiting list until after those in the first group are finished the progeamme. Participants are followed up at a three month follow up to assess their distress levels, severity of their symptoms, pain, anxiety symptoms, health-related quality of life and other aspects. What are the possible benefits and risks of participating? Participants may benefit from improvements in the quality of life, well-being and other MS- related symptoms. There are no direct risks associated with participating. Where is the study run from? Centre for Pain Research (Ireland) When is the study starting and how long is it expected to run for? March 2016 to February 2019 Who is funding the study? Irish Health Research Board and the Medical Research Charities Group Joint Funding Scheme (Ireland) Who is the main contact? Dr Chris Dwyer (Scientific) painresearch@nuigalway.ie
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History
Started
Jun 2018
Finished
May 2019