Characterisation of Pain in Patients With Musculoskeletal Disease: a Prospective, Longitudinal, Observational Study With an Embedded Feasibility Window of Opportunity Sleep Study
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Fibromyalgia
- Sponsor
- University of Oxford
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- Change in Revised Fibromyalgia Impact Questionnaire (FIQR) from baseline
- Status
- Active, Not Recruiting
- Last Updated
- 11 months ago
Overview
Brief Summary
The goal of this clinical trial is to investigate the potential benefits of a digital Cognitive Behavioural Therapy for Insomnia (dCBT-I) platform, Sleepio, in individuals suffering from fibromyalgia, a condition commonly associated with cognitive issues and sleep disorders.
The main questions this study aims to answer are:
- Does the application of Sleepio improve quality of life in individuals with fibromyalgia?
- Does the use of Sleepio improve cognitive function in individuals with fibromyalgia?
- Does the use of Sleepio enhance sleep quality in these same individuals?
- Does the use of Sleepio improve motor function in this group?
Participants will be randomly assigned to either use the Sleepio platform or standardised health advice, including sleep hygiene material. Those assigned to Sleepio will undergo a series of six 20-minute sessions over 10 weeks with a virtual therapist focusing on cognitive and behavioural strategies for improving sleep.
Participants' quality of life, cognitive function, sleep quality, and pain levels will be monitored and evaluated using online assessment tools. Additionally, a subset of participants will undergo further testing via sleep actigraphy and/or neuroimaging with MRI scans.
Researchers will compare the two groups to determine if the use of Sleepio has a positive effect on quality of life, cognitive function, and sleep quality.
Detailed Description
Fibromyalgia patients commonly experience cognitive issues such as concentration and memory difficulties and sleep disorders. Despite the prevalence of these symptoms, no established treatments currently exist. Traditional in-person Cognitive Behavioural Therapy (CBT), which focuses on modifying unhelpful thoughts and behaviours, is both expensive and challenging to deliver on a broad scale. New digital forms of CBT, specifically for insomnia (CBT-I), have shown promise in improving cognitive symptoms and sleep quality, but their effect on fibromyalgia patients is yet to be explored. The study will investigate the efficacy of 'Sleepio', an established digital CBT-I (dCBT-I) tool. Sleepio has shown effectiveness in treating insomnia and its cognitive symptoms, offering a promising approach to address similar issues in fibromyalgia. Sleepio's approach involves six 20-minute sessions over 10 weeks with a virtual therapist who employs key cognitive and behavioural strategies to enhance sleep quality. Participants in this study will be randomised in a 1:1 ratio to either treatment with Sleepio treatment or standard care with standard sleep hygiene advice. The primary outcome is quality of life measured on the Revised Fibromyalgia Impact Questionnaire (FIQR), 12 weeks following randomisation. Secondary outcomes include subjective cognition (British Columbia Cognitive Complaints Inventory, BC-CCI), objective cognitive function (tests of reaction time, working memory, processing speed), quantitative cognitive avoidance testing (QCAT), sleep quality (actigraphy, insomnia severity index (ISI), Pittsburgh Sleep Quality Index (PSQI), pain (NRS), fear of movement (Tampa Scale of Kinesiophobia) and quantitative movement assessment. Assessments will be carried out using online tools. Additionally, a subset of participants will undergo sleep actigraphy and/or neuroimaging using MRI scans for a more detailed analysis. Primary Objectives: - Assess the impact of Sleepio (dCBT-I) on quality of life (FIQR) in fibromyalgia patients. Secondary Objectives: * Assess the impact of Sleepio (dCBT-I) on subjective (BC-CCI) and objective cognitive function in fibromyalgia patients. * Investigate the effect of Sleepio on sleep quality (ISI \& PSQI) in fibromyalgia patients. * Investigate cost-effectiveness of Sleepio (dCBT-I) * Does Sleepio improve subjective and objective measures of motor function in fibromyalgia? As part of the study, participants will also be invited to join a research database for potential inclusion in future studies conducted by the research group.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Clinical diagnosis of fibromyalgia
- •Concomitant insomnia, frequent waking in the night or early morning waking
- •Self-reported difficulties with concentration or memory
- •Reliable internet access
Exclusion Criteria
- •Patients with a poor understanding of English.
- •Patients with known neurological or psychiatric conditions (other than depression or anxiety) likely to independently affect the results of pain assessment, for example peripheral diabetic neuropathy in the opinion of the research team
- •Major neuropsychiatric disorder (bipolar disorder, schizophrenia or psychotic spectrum disorders)
- •Cognitive impairment, dementia or neurodegenerative disorder
- •Recent or planned surgery
- •Current or planned night-time shift work
- •Sleep disorders such as sleep apnoea, restless leg syndrome, circadian rhythm disorder, or parasomnia
- •Taking prescribed sleep medications on more than 2 nights in past 2 weeks
- •Currently receiving other psychological therapy for insomnia
- •Pregnant or lactating
Outcomes
Primary Outcomes
Change in Revised Fibromyalgia Impact Questionnaire (FIQR) from baseline
Time Frame: 12 weeks
The revised Fibromyalgia Impact Questionnaire (FIQR), range 0-100, is a self-reported measure designed to assess the overall impact of fibromyalgia on patients' lives, capturing domains such as physical impairment, overall well-being, and the intensity of symptoms like pain, fatigue, stiffness, sleep disturbances, and cognitive problems. Higher scores indicate more severe symptoms.
Secondary Outcomes
- Changes in neurotransmitter concentration in the insular(12 weeks)
- Change in Revised Fibromyalgia Impact Questionnaire (FIQR) from baseline(52 weeks)
- Sleep quality(12 weeks)
- Change in British Columbia Cognitive Complaints Inventory (BC-CCI) from baseline(52 weeks)
- Change in Tampa Scale of Kinesiophobia (TSK) from baseline(52 weeks)
- Cost-effectiveness of dCBT-I(24 weeks)
- Changes in brain structure(12 weeks)
- Changes in brain functional connectivity(12 weeks)
- Changes in brain function(12 weeks)