Severe Asthma, MepolizumaB and Affect: SAMBA Study

Depression Clinical Trial

— SAMBA  

Official title:

The Biopsychosocial Impact of Mepolizumab in Severe Eosinophilic Asthma on Quantitative and Qualitative Emotional and Affective Outcomes in Patients and Partners

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04680611
• Other study ID #: RHM MED1740
• Status: Recruiting
• Start date: September 9, 2021
• Est. completion date: December 31, 2024

Study information

• Verified date: October 2023
• Source: University Hospital Southampton NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This is a real-life pragmatic non-randomised study to explore the impact of mepolizumab on the emotional and affective outcomes of patients with severe eosinophilic asthma and their partners. It will be conducted in two quantitative stages (Phases 1 and 2) with an additional third qualitative component (Phase 3).

Description:

This longitudinal observational study will investigate the relationship between patients' asthma control and emotional states and quality of life in patients and their partners where patients have severe eosinophilic asthma. The study will consist of three phases.

Phase 1 In order to extend our pilot study findings and help inform the second stage, investigators will gather Geneva Emotional Wheel (GEW) data from 30 patients currently treated and benefitting from mepolizumab (Nucala®). This data will be compared to the GEW data investigators have already gathered from patients with severe asthma not receiving treatment with mepolizumab (Nucala®). This will provide timely data to support a publication on the GEW findings in severe asthma and allow the description of the impact of mepolizumab (Nucala®). In addition, it will help provide power calculations for a prospective study. Parallel assessment of quality of life (SGRQ and SAQ) and anxiety and depression (HADS) will be made to evaluate the relationship between GEW, SGRQ, SAQ and HADS scores.

Phase 2 In the second stage, investigators will conduct a prospective study of 45 patients newly prescribed mepolizumab (Nucala®) and their partners measuring participants' emotional composition before and 6 and 12 months after starting treatment. The choice of 60 has been based on likely power requirements but was adjusted to 45 based in Phase 1 results. Investigators will also compare the outcomes from the GEW with other standard outcome measures (HADS, ACQ, SGRQ, SAQ, BIPQ), to establish relationship between changes in these measures and changes in GEW scores, to evaluate the utility of the GEW. This will help determine if the GEW reflects changes in asthma control or whether it is reflecting improvements that the current established instruments do not recognise and allow us to quantify the magnitude of that effect. As these patients will receive mepolizumab as part of their clinical care for a year, whilst assessment of clinical efficacy is being established, investigators will gather data on oral steroid dependent exacerbations (severe exacerbations) during this year and relate to their historic exacerbation history in the year before. Evaluation will be made as to whether the 6-month improvement in GEW scores predicts impact of mepolizumab on exacerbation reduction over the first year of administration. In addition, improvements in the GEW will be explored in relationship to systemic inflammatory impact, with measures of blood eosinophils and serum inflammatory biomarkers (Olink inflammatory panel) at baseline, 6 months and 1 year.

Phase 3 Finally, in addition, investigators will conduct qualitative research in the form of semi-structured interviews with a sub-set of couples (20 couples or less if no new information emerges from the interviews) to gain a more detailed insight and identify common key aspects in their subjective experiences, quality of life and emotional processes before starting treatment and after being on treatment with mepolizumab for 6 months.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Phase 1:

• Age 18 or over

• Having a diagnosis of severe eosinophilic asthma

• Currently on mepolizumab (Nucala®) treatment

• At least basic command of English

• Giving written informed consent

Phase 2 Patient eligibility Inclusion criteria

• Age 18 or over

• Having a diagnosis of severe eosinophilic asthma

• Scheduled to start mepolizumab (Nucala®) treatment

• At least basic command of English (for sub-study: conversational level of English that does not require a translator)

• Giving written informed consent

• Co-habiting with an intimate partner who is willing to participate in the study

Exclusion criteria

• Participated in Phase 1

• Currently on mepolizumab (Nucala®) treatment

• Major psychiatric disorder currently under treatment

• History of any major psychiatric disorder in the last 5 years, excluding depressive and anxiety disorders that can be included if treatment or change of treatment (including change in dose of medication) has not started within the last 6 months

• Any diagnosed severe comorbid chronic condition that, in the opinion of the patient's asthma physician, might impact on the patient's or partner's affective state (e.g. cancer, diabetes, heart failure, chronic liver disease, chronic kidney disease, autoimmune or neuro-degenerative disease).

• Partners only: diagnosis of severe eosinophilic asthma

• Death of spouse, main informal carer or first-degree family member within the last 3 months

• Current oral corticosteroid maintenance treatment

Partner eligibility Inclusion criteria

• Age 18 or over

• At least basic command of English (for sub-study: conversational level of English that does not require a translator)

• Giving written informed consent

• Partners: Co-habiting with an intimate partner who has severe eosinophilic asthma and is willing to participate in the study

Exclusion criteria

• Participated in Phase 1

• Major psychiatric disorder currently under treatment

• Participant self-reported history of any major psychiatric disorder in the last 5 years, excluding depressive and anxiety disorders that can be included if treatment or change of treatment (including change in dose of medication) has not started within the last 6 months.

• Participant self-reported any diagnosed severe comorbid chronic condition that, in the opinion of the patient's asthma physician, might impact on the patient's or partner's affective state (e.g. cancer, diabetes, heart failure, chronic liver disease, chronic kidney disease, autoimmune or neuro-degenerative disease).

• Diagnosis of severe eosinophilic asthma

• Death of spouse, main informal carer or first-degree family member within the last 3 months

• Current oral corticosteroid maintenance treatment

Phase 3:

Phase 3 is a qualitative study on a sample of couples from Phase 2 therefore the same exclusion criteria will apply as in Phase 2.

Related Conditions & MeSH terms

• Adjustment
• Adjustment, Emotional
• Anxiety
• Asthma
• Coping Behavior
• Depression
• Emotional Disorder
• Emotional Distress
• Emotional Dysfunction
• Emotions
• Mental Disorders
• Psychological
• Psychological Adjustment
• Psychological Disorder
• Psychological Distress
• Psychological Stress
• Psychosocial Problem
• Psychosocial Stressor
• Pulmonary Eosinophilia
• Severe Eosinophilic Asthma
• Stress, Psychological

Intervention

Other:
• no study intervention. Patients receive standard clinical care
no intervention. observational study

Locations

Country	Name	City	State
United Kingdom	Department of Respiratory Medicine, Aberdeen Royal Infirmary	Aberdeen	Grampian
United Kingdom	Glasgow Gartnavel General Hospital	Glasgow
United Kingdom	Hull University Teaching Hospitals NHS Trust	Hull	Yorkshire
United Kingdom	Portsmouth Hospitals NHS Trust	Portsmouth
United Kingdom	Judit Varkonyi-Sepp	Southampton	Hampshire
United Kingdom	Pinderfields Hospital	Wakefield	Yorkshire

Sponsors (3)

Lead Sponsor	Collaborator
University Hospital Southampton NHS Foundation Trust	Portsmouth Hospitals NHS Trust, University of Derby

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	change in Inflammatory panel and chemokines	Olink inflammatory panel and particular chemokines that are comprehensively listed at https://www.olink.com/content/uploads/2019/04/Olink-Inflammation-Validation-Data-v3.0.pdf) will be used to measure markers of systemic inflammation and assess links between affective states and systemic inflammation. In addition, Serum CCl17 and CCL26 will be measured by ELISA as these biomarkers do not feature in the Olink inflammatory panel.	Phase 2 only: change from baseline to 1 year after start of treatment
Other	lived experiences and psychological processes (using Semi-structured interviews)	Interviews to explore participants' quality of life	Phase 2 only: change from baseline to 1 year after start of treatment
Primary	Change in emotional composition (using the Geneva Emotions Wheel)	A 20-item self-report questionnaire identifying 20 discrete emotions with positive or negative valence. The intensity of each emotion can be marked on a 6-point Likert-type scale. Lower scores indicate lower intensity of emotions, higher scores indicate higher intensity of emotions. Respondents can add free text. Can be used a a variety of applications. The emotion labels used in the study have been modified with input from representatives of the target study population to ensure complete relevance to the study..	Phase 1: on enrolment. Phase 2: change to one year after start of treatment
Secondary	change in affective state (using the Hospital Anxiety and Depression Scale)	Clinical diagnostic self-report questionnaire to assess psychological distress. Consists of anxiety and depression sub-scales. It consists of seven questions for anxiety and seven questions for depression that are in mixed order in the questionnaire. Each question has four possible answers scored from 0-3. There are separate sub-scale scores for anxiety and depression each with cut-off scores 0-7: normal, 8-10: borderline abnormal and 11-21: abnormal. The HADS is a self-report tool and takes 2-5minutes to complete.	Phase 1: on enrolment. Phase 2: change from baseline to 1 year after start of treatment
Secondary	change in self-reported asthma symptom control (using the Asthma Control Questionnaire)	6-item clinical questionnaire to establish self-assessed asthma control (questions 1-6) and lung function measured by healthcare professional (item 7). 6 of the questions are patients self-report about their asthma during the previous week regarding symptoms and bronchodilator use. Responses are given on a 7-point scale (0=no impairment, 6= maximum impairment). The ACQ score is the mean of all the questions and therefore between 0 (totally controlled) and 6 (severely uncontrolled). In general, patients with a score below 1.0 have adequately controlled asthma and above 1.0 their asthma is not controlled. Patients with a score between 0.75 and 1.25 have borderline of adequate control. The smallest clinically important change is 0.5.	Phase 1: on enrolment. Phase 2: change from baseline to 1 year after start of treatment
Secondary	change in functioning and quality of life (using the St Georges Respiratory Questionnaire)	Clinical questionnaire to assess disease impact on quality of life. QThe questionnaire has two parts. Part 1 (Questions 1 to 8) covers the patients' recollection of their symptoms over the preceding period (range 1 month to 1 year). Part 2 (Questions 9 to 16) is related to the patients' current state. The Activity score covers functioning related to patients' daily physical activity. The Impacts score relates to psychosocial functioning. Although this component relates partly to physical symptoms, it also correlates quite strongly with exercise performance, breathlessness and disturbances of mood (anxiety and depression), therefore it is the broadest component of the questionnaire, covering the whole range of disturbances that respiratory patients experience in their lives. Scoring is weighted, gihres scores indicate worse outcomes.	Phase 1: on enrolment Phase 2: change from baseline to 1 year after start of treatment
Secondary	change in asthma-related quality of life (using the Severe Asthma Questionnaire)	Questionnaire assessing the impact of severe asthma and the effects of treatment on patient's self-reported health-related quality of life. The questionnaire produces two scores: the SAQ score is the aggregation of 16 different QoL domains and the SAQ-global score is the figure given on a 100-point scale. Higher scroes indicate higher adverese impact on the responder's life.The scale takes between 3 to 6 minutes to complete, but completion time reduces on subsequent occasions.	Phase 1: on enrolment Phase 2: change from baseline to 1 year after start of treatment
Secondary	change in illness perception (using the Brief Illness Perception Questionnaire)	Questionnaire assessing the beliefs individuals have about the cause, controllability and impact on them of the illness. Comprises 9 questions. 8 questions use a Likert scale response. Question 9 can be answered by free text about the perceived cause of illness.	Phase 2: change from basline to 1 year after start of treatment