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Acceptance and Commitment Therapy for Muscle Disease

Acceptance and Commitment Therapy for Muscle Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02810028
Acronym
ACTMuS
Enrollment
155
Registered
2016-06-22
Start date
2016-07-31
Completion date
2019-01-31
Last updated
2019-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Diseases

Keywords

Limb girdle muscular dystrophy, Becker's muscular dystrophy, Facioscapulohumeral muscular dystrophy, Inclusion-body myositis, Acceptance and Commitment Therapy, ACT

Brief summary

In adults, muscle diseases are usually chronic long-term conditions that do not have a definitive cure. Supportive care has been shown to reduce complications from muscle disease and improved survival in some cases. However, there has been limited research to evaluate interventions that may improve quality of life (QoL) with this patient group. The QoL of those with MD is not just affected by the severity of their MD but also a variety of psychological variables. Based upon the knowledge of these psychological variables the investigators feel that a particular type of psychological intervention known as acceptance and commitment therapy (ACT) could potentially improve QoL in those with MD. The investigators therefore propose to test whether ACT does in fact improve QoL in those with MD by randomising 154 patients to receive either standard medical care plus a guided self-help ACT programme, or standard medical care only.

Detailed description

Previous research has shown that while QoL is determined by the severity of the MD, this does not explain all aspects of the reduced QoL of those with MD. Previous research suggested that a cognitive behavioural approach using Acceptance and Commitment Therapy (ACT) would best suit those with MD. A pilot study of this approach in seven participants with MD was promising, and has led to this definitive trial of ACT. The aim of this study is to determine the efficacy of an ACT intervention to improve the QoL of individuals with MD. Patients with one of the following muscle diseases will be recruited: limb girdle muscular dystrophy, dystrophinopathies resulting in a Becker' muscular dystrophy phenotype, facioscapulohumeral muscular dystrophy and inclusion body myositis. Patients will be recruited primarily through muscle clinics at King's College Hospital (KCH) and The Royal London Hospital (RLH) but also via Muscular Dystrophy UK (MDUK) and UK registries of patients with these muscle diseases.

Interventions

BEHAVIORALAcceptance and Commitment Therapy (ACT)

Acceptance and Commitment Therapy (ACT) is a form of cognitive behavioural therapy focused explicitly on promoting psychological flexibility. An ACT programme suits the aims of the study because it targets avoidance of distress, promotes acceptance of illness through motivating meaningful activity outside of illness, improves the processes that underlie beliefs rather than by directly challenging beliefs, thus reducing possible trivialisation of the understandable distress caused by living with MD.

Sponsors

King's College London
CollaboratorOTHER
Barts & The London NHS Trust
CollaboratorOTHER
Muscular Dystrophy Association
CollaboratorOTHER
University Hospital Southampton NHS Foundation Trust
CollaboratorOTHER
King's College Hospital NHS Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Diagnosed with one of four specific muscle diseases on the basis of diagnostic criteria: 1. Limb girdle muscular dystrophy; symptomatic limb girdle muscular dystrophy genetically or pathologically proven 2. Dystrophinopathies resulting in a Becker' muscular dystrophy phenotype (excluding Duchenne muscular dystrophy) with pathology or genetic diagnosis 3. Facioscapulohumeral muscular dystrophy diagnosed clinically with specific genetic abnormality in the subject or their family 4. Inclusion body myositis clinic-pathologically defined, clinically defined or probable IBM based on ENMC research diagnostic criteria 2013 (submitted) 2. duration of muscle disease greater than six months 3. over the age of 18 years 4. access to the internet and a computer on which they can receive the intervention materials 5. HADS scores \> 8 for depression or \>8 for anxiety

Exclusion criteria

1. Major active co-morbidities unrelated to muscle disease such as arthritis, respiratory disease, cardiovascular disease 2. Unstable complications of muscle disease including: 1. neuromuscular respiratory weakness 2. cardiomyopathy 3. Cognitive impairment that prevents comprehension of the questionnaires; assessed using the Montreal Cognitive Assessment 4. Unable to read English questionnaires 5. Major diagnosed active mental health co-morbidities e.g. psychosis, major depression, obsessive compulsive disorder, active suicide risk 6. Current or recent participation in other treatment intervention studies (\< 4 weeks after completion) 7. Currently receiving psychological support or psychotherapy

Design outcomes

Primary

MeasureTime frameDescription
Individualised Neuromuscular Quality of Life Questionnaire (INQoL) - Life areas9 weeks post randomisationMeasures impact of MD on life areas: activities, independence, social functioning, emotional functioning and body image.

Secondary

MeasureTime frameDescription
Patient rating of treatment satisfaction9 weeks post randomisationMeasures patient's satisfaction with the treatment they have received.
Committed Action Scale (CAS)9 weeks post randomisationMeasures commitment towards goals.
IBM Functional Rating Scale9 weeks post randomisationAssesses function in people with Inclusion Body Myositis.
Patient Global Impression of Change scale (PGIC)9 weeks post randomisationAssesses patient's own impression of change during the course of the study.
Stanford Health Assessment Questionnaire Disability Index (HAQ-DI)9 weeks post randomisationMeasures functional impairment.
Acceptance and Action Questionnaire (AAQ-II)9 weeks post randomisationMeasures psychological flexibility.
Individualised Neuromuscular Quality of Life Questionnaire (INQoL) - Symptom impact domains9 weeks post randomisationMeasures the impact of key muscle disease symptoms: weakness, fatigue and pain.
Work and Social Adjustment Scale (WSAS)9 weeks post randomisationAssesses how much symptoms interfere with participation in life i.e. work, home management, social, private and relationships.
Hospital Anxiety and Depression Scale (HADS)9 weeks post randomisationMeasures mood.
Mindfulness Attention Awareness Scale (MAAS)9 weeks post randomisationMeasures dispositional open awareness of and attention to the present moment.

Other

MeasureTime frameDescription
Adult Ambulatory Neuromuscular Assessment (AANA)Baseline onlyAn adult version of the North Star Ambulatory Assessment that measures motor function.
Manual Muscle Strength Testing (MMST)Baseline onlyMeasures muscle strength.
6-minute timed walk testBaseline onlyMeasures mobility.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026