Behaviour change
Behavioralhealthy conversations to support behaviour change
Other names: healthy conversations
NCT Number: NCT06513117
Multimorbidity is a significant issue for many patients with difficult asthma. With patients, we have co-designed a multimodal intervention comprising prescribed exercise, dietary support, breathing pattern retraining and behaviour change to target multimorbidity in difficult asthma
Trial opening soon.
Get Notified18 year–80 year
All sexes
Interventional
Not applicable
Multimorbidity (living with more than 2 additional health conditions) is very common for patients with Difficult Asthma, and has an impact on symptom burden and exacerbation frequency. The investigators want to find out if a personalised intervention (i.e. exercise training, behavioural change support, breathing retraining and dietary and emotional self-management support) to address mutimorbidity is feasible and tolerable and can improve asthma symptoms in difficult asthma. The investigators also want to find out if this intervention continues to benefit patients and help them to continue lifestyle changes after the intervention has finished.
The aim of this exercise training will be to improve fitness. The investigators believe that increases in physical fitness will improve symptom burden through reductions in inflammation and improved resilience. The aim of the dietary and emotional self-management support is to help participants develop their own solutions for healthy eating and keeping emotionally well. The aim of the behavioural change programme is to help participants continue these lifestyle changes post intervention and manage the challenges of living with difficult asthma alongside other multiple health conditions.
This is a pilot study, so all participants will receive the intervention.
Participants with difficult asthma and multimorbidity (more than 2 additional long term health conditions alongside asthma) will be invited to take part in the study. Participants will undertake in a 6-month/ 24 week supervised multimodal health improvement programme (combining exercise training, behavioural change support, breathing retraining and dietary and emotional self-management support. This programme will run alongside their treatment. The programme will be delivered by highly trained Health Guides, who are trained exercise professionals and have received additional training including how to support people to change their behaviour to be able to look after their own physical and emotional wellbeing by themselves in the long run. During the first 12 weeks, participants will take part in 2 community gym based sessions and 1 home based exercise session every week, all supervised by the Health Guide (in person in the gym and through a video or telephone call at home). For weeks 12-24, they will complete 1 community gym based session and 1 virtual/home based session, supervised by the Health Guide, and 1 session on their own. The sessions with the Health Guide will consist of:
It is safe to exercise and possible benefits include improved symptoms and quality of life. After exercising some people may feel achy or sore, but this should subside within a day or two. It is normal to feel short of breath during exercise. Occasionally, asthma symptoms are exacerbated briefly during exercise-this will be monitored for during the early supervised exercise sessions, and participants will be advised to take a dose of their reliever if needed.
During blood sampling, participants may feel discomfort due to the needle and may have bruising, bleeding or swelling at the blood sample site. Participants may feel faint and dizzy while blood is being drawn and there is a slight risk of infection.
Sometimes conversations about habits or emotional wellbeing might be a bit emotional but the Health Guide will be trained in how to provide support should this happen and to discuss further steps with participants if and when it is needed.
The study will open in the autumn of 2024, and will run for 18 months, with participants followed up for 12 months. The BMA James Trust is funding the study, with additional support from the NIHR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Aged 18 to 80 years Able and willing to give informed consent Diagnosis of asthma determined by
Exclusion criteria
healthy conversations to support behaviour change
Other names: healthy conversations
Guidance on healthy eating
guidance on breathing pattern in exercise
Exercise intervention prescribed to participant fitness level
Time frame: pre and post intervention, at 12 month follow up
Primary feasibility outcome is feasibility and acceptability to patients. Primary clinical endpoint outcome measure will be a minimal clinically significant improvement in ACQ 6 score (>0.5). Score scale is from 0-6, with < 1.5 demonstrating good asthma symptom control.
Time frame: pre and post intervention, at 12 month follow up
Increase in exercise capacity as assessed through oxygen uptake of > 2ml/kg/min at anaerobic threshold (AT) on maximal, symptom limited, incremental shuttle walk test.
Time frame: pre and post intervention, at 12 month follow up
32 questions scored on Likert scale 1-7. Score is mean of 32 answers, range 1-7 (higher =better quality of life
Time frame: pre and post intervention, at 12 month follow up
number of asthma exacerbations requiring oral corticosteroid treatment
Contact information is provided by the study sponsor or research team.
University of Southampton
Other
LIving BEtteR With asThma studY: A Multimodal Intervention to Address Multimorbidity in Difficult Asthma
Acronym: LIBERTY
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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