Personalized Exercise Therapy and Self-management Support for Patients With Multimorbidity (MOBILIZE)

Improving Health in People With Multimorbidity: a Paradigm Shift in Health Care From Disease-based Curative Models to Personalized Exercise Therapy and Self-management

Chronic conditions such as knee or hip osteoarthritis (OA), chronic obstructive pulmonary disease (COPD), heart failure (HF), coronary heart disease (CHD), hypertension, type 2 diabetes mellitus (T2DM) and depression are among the leading causes of global disability and affect hundreds of millions of people around the world. In recent years, multimorbidity, commonly defined as the co-occurrence of at least two chronic conditions, has also gained interest due to its substantial impact on the person and society.

Despite the significant burden of multimorbidity, little is known about how to treat this effectively. A 2016 Cochrane systematic review found that interventions targeting populations with specific combinations of conditions and addressing specific problems such as functional difficulties may be more effective. Exercise therapy is a treatment addressing functional limitations that is a safe and effective treatment of at least 26 chronic conditions, including OA, HF, CHD, hypertension, T2DM, COPD and depression. Furthermore, self-management support is increasingly recognized as an essential component of interventions to improve outcomes in patients living with multimorbidity and to support the long-term adherence to exercise. A new systematic review found that exercise seems effective in people with multimorbidity (the conditions included in the current study), however highlighting the need for further high-quality RCTs.

The aim of this randomized controlled trial (RCT) is to investigate the effects of a personalized exercise therapy and self-management support program in addition to usual care on self-reported, objectively measured and physiological outcomes in people with multimorbidity (i.e. at least two of the following conditions: OA (knee or hip), heart condition (HF or CHD), hypertension, T2DM, COPD and depression). The primary endpoint is 12 months, but 4- and 6-month follow-ups are included as well and a 12-month health economic evaluation of the program will be conducted.

Prior to the RCT, a feasibility trial of 20 people with multimorbidity, all undergoing the personalized exercise therapy and self-management support program, will be conducted using the same methods as in the RCT, but primarily focusing on feasibility outcomes (recruitment, retention, adherence to treatment, burden of outcomes, improvements in outcomes, adverse events). This will start recruitment in Feb 2021 and end August 2021.

The MOBILIZE project has received funding from several foundations, including the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (grant agreement No 801790).

Study Overview

• Status: Active, not recruiting
• Conditions: Depression; Heart Failure; Hypertension; Chronic Obstructive Pulmonary Disease; Osteoarthritis, Knee; Coronary Heart Disease; Osteoarthritis, Hip; Type2 Diabetes
• Intervention / Treatment: Behavioral: Personalized exercise therapy and self-management support program; Other: Usual care

Detailed Description

Chronic conditions such as knee or hip osteoarthritis (OA), chronic obstructive pulmonary disease (COPD), heart failure (HF), coronary heart disease (CHD), hypertension, type 2 diabetes mellitus (T2DM) and depression are among the leading causes of global disability and affect hundreds of millions of people around the world. In recent years, multimorbidity, commonly defined as the co-occurrence of at least two chronic conditions, has also gained interest due to its substantial impact on the person and society. In general, multimorbidity affects more than half of all people with chronic conditions. Two out of three people with OA have comorbidities, with HF, CHD, hypertension, T2DM, COPD and depression being some of the most common.

People with multimorbidity account for 78% of all consultations in primary care and multimorbidity is associated with poorer function and quality of life, depression, intake of multiple drugs and increased health care utilization, with some studies demonstrating an almost exponential relationship between the number of chronic conditions and their health care costs. Furthermore, we know from qualitative research that treating one condition at a time is inconvenient, inefficient and unsatisfactory for the person with the chronic conditions and his or her health care provider. Most research so far has excluded people with multimorbidity, due to its focus on only one specific condition, and most of the health care sector manages each individual condition on its own instead of the person, highlighting the negative impact of the current disease-based curative models on multimorbidity. With a population that is ageing, and a significant number of people with multimorbidity being younger than 65 years of age, the proportion of people with multimorbidity is increasing rapidly, emphasizing the need to take action to deal with the increasing burden of chronic conditions and multimorbidity through treatment and prevention.

Identifying and developing effective and affordable treatment strategies to deal with the global burden of chronic conditions and multimorbidity is a major focus of modern health care around the world. Despite the significant burden of multimorbidity, little is known about how to treat this effectively. A 2016 Cochrane systematic review found that interventions targeting populations with specific combinations of conditions and addressing specific problems such as functional difficulties may be more effective. A treatment addressing functional limitations that is able to improve symptoms in at least 26 chronic conditions, including OA, HF, CHD, hypertension, T2DM, COPD and depression is readily available. This treatment is exercise therapy, which is effective, safe and supported by substantial evidence in patients with knee and hip OA, HF and CHD, hypertension, T2DM, COPD, depression and a range of other chronic conditions. A new systematic review found that exercise seems effective in people with multimorbidity (the conditions included in the current study), however highlighting the need for further high-quality RCTs. Furthermore, self-management support is increasingly recognized as an essential component of interventions to improve outcomes in patients living with multimorbidity. There is increasing evidence that effective management of multimorbidity requires the active participation by patients in the care process. Self-management support interventions have been shown to change health behaviors, improve health status, and reduce health care utilization and costs. Self-management support is centered on enabling patients to develop a set of behavioral skills and abilities to help them navigate a range of disease management tasks across different chronic conditions.

In an RCT of people with knee OA, published in the New England Journal of Medicine, we found that 3 out of 4 patients eligible for total knee replacement improved enough from self-management support, supervised exercise therapy and other non-surgical treatments to postpone surgery for at least one year. Furthermore, in patients with T2DM, 56% did not take antidiabetic medication after 1 year of supervised exercise therapy, self-management support and diet. Together, these studies indicate the potential of combining exercise, self-management and other treatments to reduce the need for surgery and medication. A recent cohort study found that an eight-week exercise and self-management program demonstrated similar improvements in health outcomes for people with OA and the comorbidities included in the current study as for people without comorbidities.

Altogether, this highlights exercise therapy and self-management support as viable treatment options for people with multimorbidity, but the evidence supporting this is of low quality and more high-quality RCTs are needed to improve care for the millions of people suffering from multimorbidity worldwide.

The overall aim of the MOBILIZE project is to empower patients with multimorbidity to take a more active role in their health care through a personalized exercise therapy and self-management support program so that they may reduce symptoms of the individual conditions, increase quality of life and physical function and prevent development of other chronic conditions. To ensure relevance to the patients and the health care system and to make sure that the project is implementable in clinical practice afterwards, strong interdisciplinary collaboration involving many different scientific methodologies and a high degree of patient involvement throughout the entire research process are at the heart of the project. The MOBILIZE project has received funding from several foundations, including the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (grant agreement No 801790). Building on the Medical Research Council's framework for the development and evaluation of complex interventions, the MOBILIZE project has four phases. During the first phase of the project, outcomes and biomarkers that predict better health outcome from different types of exercise therapy and exercise characteristics associated with a better outcome in people with different combinations of chronic conditions will be identified through exploratory observational cohort studies of people with osteoarthritis who have undergone an 8-week exercise therapy and education program in Denmark (GLA:D) as well as scoping reviews, systematic reviews and meta-analyses that summarize the existing evidence. Subsequently, in phase 2, a 12-week exercise therapy and self-management support program will be developed based on existing recommendations for exercise and strategies to facilitate behavioral changes. To ensure a high degree of patient and provider involvement, focus group interviews will be conducted with patients with multimorbidity, health care providers and other relevant stakeholders to acquire their views and perspectives on multimorbidity and exercise. Once this phase is completed, the exercise therapy and self-management support program will be tested in a feasibility trial involving 20 patients with multimorbidity (recruited from Feb 2021 and onwards). The same procedures and outcomes as in the subsequent RCT will be used, and data will be collected at baseline and after the 12-week intervention. The feasibility trial will primarily focus on feasibility outcomes (recruitment, retention, adherence to treatment, burden of outcomes, improvements in outcomes, adverse events), using a red/amber/green traffic light system, guiding the progression to the subsequent RCT. Experiences from the feasibility trial will be used to evaluate and implement any adjustments that need to be made prior to commencing the RCT (described in details in the current trial registration). The RCT corresponds to phase 3, while phase 4 focuses on developing a model for implementation of the personalized exercise therapy and self-management support program in clinical practice, if supported by the study findings.

The aim of the RCT described in this clinical trial registration is to investigate the effects of a personalized exercise therapy and self-management support program in addition to usual care on self-reported, objectively measured and physiological outcomes in people with multimorbidity (i.e. at least two of the following conditions: OA (knee or hip), heart condition (HF or CHD), hypertension, T2DM, COPD and depression). The primary endpoint is 12 months, but 4- and 6-month follow-ups are included as well and a 12-month health economic evaluation of the program will be conducted. The 4-month follow-up corresponds to immediately after the intervention, including the time it takes to conduct the baseline measurements and be enrolled in the group-based program.

The primary study hypothesis is that a personalized exercise therapy and self-management support program in addition to usual care will improve quality of life more than usual care alone when measured at 12 months with concurrent positive effects on secondary outcomes. Furthermore, it is hypothesized that the program will be cost-effective at 12 months.

People will be recruited via the recruitment centers mentioned in this registration as well as via self-referral (Facebook posts, newspaper articles and flyers).

People who only fulfil some of the eligibility criteria (aged 18 years or above, at least two of the relevant conditions and do not have psychosis disorders, post-traumatic stress disorder, Obsessive Compulsive Disorder, attention deficit hyperactivity disorder, autism, anorexia nervosa/bulimia nervosa or an abuse or other reasons for exclusion) or people fulfilling all eligibility criteria, but unwilling to participate in the RCT, will be offered participation in an observational cohort study where only the self-reported outcomes are completed. Recruitment for the cohort will start and end with the recruitment for the RCT.

• Study Type: Interventional
• Enrollment (Actual): 228
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Søren T Skou, PT, MSc, PhD; Phone Number: +4523708640; Email: stskou@health.sdu.dk
• Study Contact Backup: Name: Mette Dideriksen, MSc; Email: mdideriksen@health.sdu.dk

Study Locations

• Denmark
  • Holbæk, Denmark
    • Holbæk Sygehus
  • Holbæk, Denmark
    • Læge Poul Erik Holst
  • Kirke Hvalsø, Denmark
    • Lægehuset Tolskovvej
  • Køge, Denmark
    • Department of Orthopedics, Zealand University Hospital
  • Nakskov, Denmark
    • Community Clinic
  • Næstved, Denmark
    • Department of Orthopaedic Surgery, Næstved Hospital
  • Næstved, Denmark
    • Department of Pulmonology, Næstved Hospital
  • Næstved, Denmark
    • Lægehuset Ostenfeldt
  • Næstved, Denmark
    • Psychiatric Clinic Næstved
  • Roskilde, Denmark
    • Community Psychiatry Roskilde
  • Roskilde, Denmark
    • Department of Cardiology, Zealand University Hospital
  • Roskilde, Denmark
    • Lægerne Algade 17
  • Slagelse, Denmark, 4200
    • Department of Cardiology and Endocrinology, Slagelse Hospital
  • Slagelse, Denmark, 4200
    • Lægerne Reventlow og Wolfhagen
  • Slagelse, Denmark, 4200
    • Psychiatric Hospital West, Slagelse
  • Slagelse, Denmark
    • Nykøbing Falster County Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• At least two of the following conditions: OA (knee or hip), COPD, heart condition (HF or CHD), hypertension, T2DM, depression (having other comorbidities does not exclude a patient)
• Adults aged 18 years or above
• Able to walk 3 meters without any assistance
• A score of 3 or above on the Bayliss' Disease Burden: Morbidity Assessment by Self- Report scale for at least one of the conditions listed above and a score of 2 or above for at least one of the other listed conditions
• Willingness and ability to participate in a 12-week supervised exercise therapy and self- management support program twice a week

Exclusion Criteria:

• Participation in supervised systematic exercise for one of their diseases within the last 3 months
• Patients with an unstable health condition or at risk of serious adverse events as evaluated by a medical specialist
• Patients categorized as Class IV on the New York Heart Association (NYHA) Functional Classification scale
• Terminal patients and patients with life expectancy of less than 12 months
• Patients with psychosis disorders, post-traumatic stress disorder, Obsessive Compulsive Disorder, attention deficit hyperactivity disorder, autism, anorexia nervosa/bulimia nervosa and patients with dependency disorders
• Other reasons (unable to understand Danish, mentally unable to participate, etc.)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Personalized exercise therapy and self-management program in addition to usual care; Participants randomized to the personalized exercise therapy and self-management support program will participate in a 12-week program tailored to people with multimorbidity at one of the intervention sites. The program will consist of 24 exercise therapy and self-management sessions distributed across the program (twice weekly, each lasting around 1.5 hour). Furthermore, this group will receive the treatment described under usual care below.	Behavioral: Personalized exercise therapy and self-management support program; See description under Arms; Other: Usual care; See description under Arms
Active Comparator: Usual care alone; Usual care is the care that the participants would receive had they not participated in the study, i.e. treatments or services that are routinely provided in the settings from which the participants are recruited. Participants will continue their current treatment, if needed, and be allowed to receive other treatments if their general practitioner or specialist finds it relevant for their particular comorbidities.	Other: Usual care; See description under Arms

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
EQ-5D-5L, the descriptive index	The descriptive index of the EuroQol-5 Domain 5-level questionnaire (EQ-5D-5L) measures the patient's self-rated health status. Ranging from -0.624 to 1, higher is better. This will also allow for a later cost-effectiveness analysis. Assessed at baseline, 4, 6 and 12 months. All visits (baseline, 4, 6 and 12 months) will be included in the analysis.	Primary endpoint: Change from baseline to 12 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
6-minute walk test	The walking distance covered over a time of 6 minutes. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Burden of illness measure	The burden of illness measure developed by Bayliss et al. measures how much illness affects the individual's daily activities (on a 1-5 scale for each individual condition, higher is worse, summed to a total score for all conditions, with an upper limit depending on the number of conditions included). Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
30-second chair-stand test	The number of chair stands completed in 30 seconds. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Depression Scale	Personal Health Questionnaire Depression Scale (PHQ-8). Ranging from 0-24 points, higher is more severe depression. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Anxiety	General Anxiety Disorder-7 (GAD-7). Ranging from 0-21, higher is more severe anxiety. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Self-Efficacy	Self-Efficacy for Managing Chronic Disease 6-item Scale. Mean of 6 items, ranging from 1 to 10, higher scores indicating higher self-efficacy. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Overall functioning and disability	12-item WHO Disability Assessment Schedule 2.0 (WHODAS 2.0). Ranging from 0 (no disability) to 100 (full disability). Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Adverse events	Adverse events (AE) and serious adverse events (SAE) will be recorded at all follow-ups by asking the participants about potential AEs using open-probe questioning to ensure that all AEs are recorded. Furthermore, the medical records of the patients will be checked at the primary endpoint (12 months) for all AEs occurring from inclusion until the 12 months follow-up. AEs will be classified according to the Food and Drug Administration definition of an SAE and recorded, categorized and assessed for severity independent of whether or not there is a causal relationship with study treatments. Assessed at 4, 6 and 12 months.	Primary endpoint: 12 months
Steps per day	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Minutes/day spent being physically active with at least light intensity	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
EQ-5D-5L, the subscale EQ VAS	The EQ visual analogue scale (EQ VAS) evaluates the patient's self-rated health on a 0-100 vertical visual analogue scale, higher score is better. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Mortality	Mortality will be recorded at 12 months via medical records	Primary endpoint: 12 months

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Isometric knee-extension strength	Isometric knee-extension strength assessed using a hand-held dynamometer. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Balance	Tandem 30-second balance test. Assessing balance in 30-second with 10 seconds in each of the 3 different positions (parallel feet, semi-tandem and tandem stand) resulting in a score from 0-30, higher is better. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Pain (yes/no) in left and right knee and hip + worst joint if more than one	Left/right knee/hip pain + worst joint if more than one. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Stress	Perceived Stress Scale (4-item version). Ranging from 0-16, higher is more stressed. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Systolic and diastolic blood pressure	Blood pressure after 5 minutes of rest. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Concentration of cholesterol (HDL and LDL) and triglyceride	Levels of cholesterol (HDL and LDL) and triglyceride. Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months
Concentration of Fasting glucose	Levels of fasting glucose. Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months
Concentration of Fasting insulin	Levels of fasting insulin. Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months
Concentration of HbA1c	Levels of HbA1c. Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months
Weight	Weight in kg. measured with a scale. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Adapted Fried Frailty and pre-frailty criteria	Frailty and pre-frailty assessed by the Adapted Fried Frailty and pre-frailty criteria. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Fatigue	One-item self-reported fatigue. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Disease-specific treatment	Self-reported disease-specific treatment. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Knee/hip pain, VAS	Average knee/hip pain during the last 7 days on a 0-100 visual analogue scale for worst joint (higher is worse pain, only for patients reporting knee/hip pain). Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Patient Acceptable Symptom State (PASS)	"Thinking about your quality of life, would you consider your current health as satisfying? With quality of life, you should consider your activities of daily living, sport and recreational activities, personal care, level of pain, and any anxiety or depression." Answered by "yes" or "no". Assessed at 4, 6 and 12 months.	Primary endpoint: 12 months
Patient-reported treatment failure	Only answered by patients answering "no" to PASS. "Would you consider your current state as being so unsatisfactory that you consider the treatment to have failed?". Answered by "yes" or "no". Assessed at 4 and 12 months.	Primary endpoint: 12 months.
Adherence	Adherence to intervention protocol of the study assessed as the number of exercise and self-management support sessions attended out of the total number of sessions available. Assessed at 4 months.	Primary endpoint: 4 months
Other treatment during follow-up	Assessed by asking the patient about changes in their pharmacological treatment as well as any other treatments that they have received outside the study since the last assessment. If the patient answers yes, questions on details of the changes and other treatments will be asked. Assessed at 4, 6 and 12 months.	Primary endpoint: 12 months
Work status	"What is your current work status?" The patients choose one of several categories (e.g. "Working", "On sick leave, full time" and "Pensioner". Assessed at baseline, 4, 6 and 12 months.	12 months.
Smoking	"How many cigarettes did you smoke in the last 7 days?" Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: 12 months
Questionnaire burden (only feasibility study)	"Did you find the questionnaire so burdensome that you would not participate in the study again?" Answered "yes"/"no". Assessed at baseline and 4 months.	Primary endpoint: 4 months
Assessment burden (only feasibility study)	"Did you find the assessments so burdensome that you would not participate in the study again?" Answered "yes"/"no". Assessed at baseline and 4 months.	Primary endpoint: 4 months
Isometric handgrip strength	Isometric handgrip strength assessed using a hand-held dynamometer. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Multimorbidity Treatment Burden	Multimorbidity Treatment Burden Questionnaire. Ranging from 0-100, higher is worse. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Short form of Patient Activation Measure (PAM)	Short form of Patient Activation Measure (PAM). Ranging from 0-100, higher scores indicating higher levels of patient activation. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Bodily pain	The number of self-reported body sites with pain in the previous 24 hours reported on a region-divided body chart of the front (A) and back (B) sides of the body. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Sedentary behaviour	Daily sedentary behaviour (one item). Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Individual items from the 12-item WHODAS 2.0	The 12 individual items from WHO Disability Assessment Schedule 2.0. Ranging from 1 to 5, higher score is worse. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Spirometry (FEV1)	Spirometry (MedikroPro) will be used to measure forced expiratory volume in first second in liter (FEV1).Assessed at baseline.	Only assessed at baseline.
Self-reported physical activity level	Weekly physical activity (two items). Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Global Perceived Effect (GPE)	Global Perceived Effect (GPE) for physical activity level, activities of daily living and quality of life. Answered on 7-point Likert scale ranging from (1) "Much better, an important improvement" to (7) "Much worse, an important deterioration", higher score is worse. Assessed at 4, 6 and 12 months.	Primary endpoint: 12 months
Falls	Over the last 4 months, have you ever been falling? "2months" at 6-month follow-up and "6 months" at the 12-month follow-up. (A fall is defined as an event resulting in you inadvertently coming to rest on the ground or another lower level, with or without loss of consciousness or injury). Never; Once; Twice; Three times or more. Assessed at 4, 6 and 12 months.	Primary endpoint: 12 months
Fear of falling	How concerned are you that you might fall? Not at all concerned; Somewhat concerned, Fairly concerned, Very concerned. Assessed at 4, 6 and 12 months.	Primary endpoint: 12 months
Sedentary activity: Time spent on sedentary activities	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Light physical activity: Time spent on light intensity activities	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Moderate physical activity: Time spent on moderate intensity activities	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Vigorous physical activity: Time spent on vigorous intensity activities	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Moderate to vigorous physical activity: Time spent on moderate to vigorous intensity activities	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Adherence to the World Health Organization (WHO) physical activity recommendations, i.e. ≥150 min. MVPA or ≥75 min. VPA weekly activities	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Sleep, objectively measured	Objectively measured sleep assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Sleep quantity, self-reported	Self-reported average sleep quantity. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Modified Karolinska Sleep Questionnaire	Sleep quality will be measured by the Modified Karolinska Sleep Questionnaire (4 items). Ranging from 4 to 24, lower is worse sleep quality. Assessed at baseline, 4, 6 and 12 months.	Primary endpoint: Change from baseline to 12 months
Vigorous Intermittent Lifestyle Physical Activity (VILPA): Time spent on VILPA intensity activities	Objectively measured physical activity assessed using combined wearable thigh and wrist accelerometers. Assessed at baseline, 4 and 12 months.	Primary endpoint: Change from baseline to 12 months
Concentration of high-sensitivity C-reactive protein (hs-CRP)	Levels of the inflammatory marker high-sensitivity C-reactive protein (hs-CRP). Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months
Concentration of Tumor necrosis factor (TNF)	Levels of the inflammatory marker Tumor necrosis factor (TNF). Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months
Concentration of Interleukin 6 (IL-6)	Levels of the inflammatory marker Interleukin 6 (IL-6). Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months
Concentration of Interleukin-1 receptor antagonist (IL-1ra)	Levels of the inflammatory marker Interleukin-1 receptor antagonist (IL-1ra). Assessed at baseline and 4 months.	Primary endpoint: Change from baseline to 4 months

Collaborators and Investigators

• Sponsor: University of Southern Denmark
• Collaborators: Zealand University Hospital; Holbaek Sygehus; Naestved Hospital; Nykøbing Falster County Hospital; Slagelse Hospital; Association of Danish Physiotherapists; European Research Council; Roskilde Municipality; Lolland Municipality; Psychiatric Hospital West, Slagelse; Næstved, Slagelse and Ringsted Hospitals' Research Fund; The Danish Health Confederation through the Development and Research Fund; FysioDanmark Holbæk; Lægerne Reventlow og Wolfhagen, Slagelse; Lægerne Algade 17, Roskilde
• Investigators: Principal Investigator: Søren T Skou, PT, MSc, PhD, Næstved, Slagelse and Ringsted hospital and University of Southern Denmark; Study Chair: Uffe Bødtger, MD, Department of Pulmonology, Næstved Hospital; Study Chair: Peter Gæde, MD, Department of Cardiology and Endocrinology, Slagelse Hospital; Study Chair: Manuel J Bieder, MD, Department of Orthopaedic Surgery, Næstved Hospital; Study Chair: Sidse Arnfred, MD, Psychiatric Hospital West, Slagelse; Study Chair: Christine Bodilsen, PT, MSc, PhD, Municipality of Roskilde; Study Chair: Jan A Overgaard, PT, MSc, Municipality of Lolland; Study Chair: Alessio Bricca, MSc, PhD, Næstved, Slagelse and Ringsted hospital and University of Southern Denmark; Study Chair: Madalina Jäger, MSc, PhD, Næstved, Slagelse and Ringsted hospital and University of Southern Denmark; Study Chair: Christian S Christiansen, MD, Nykøbing Falster County Hospital; Study Chair: Anne Merete B Soja, MD, PhD, DMSc, Holbaek Sygehus; Study Chair: Niels Eske Bruun, MD, Department of Cardiology, Zealand University Hospital, Roskilde; Study Chair: Johan L Reventlow, MD, Lægerne Reventlow og Wolfhagen, Slagelse; Study Chair: Andreas Heltberg, MD, PhD, Lægerne Algade 17, Roskilde; Study Chair: Lau C Thygesen, MSc, PhD, University of Southern Denmark; Study Chair: Poul Erik Holst, MD, Læge Poul Erik Holst, Holbæk; Study Chair: Rita M Andersen, MSc, Psychiatric Clinic Næstved; Study Chair: Amir Pasha Attarzadeh, MD, Department of Orthopedics, Zealand University Hospital, Køge; Study Chair: Mickey T Kongerslev, MSc, Community Psychiatry Roskilde; Study Chair: Louise Richelieu, MD, Lægehuset Tolskovvej, Hvalsø; Study Chair: Signe Aspelin, MD, Lægehuset Ostenfeldt, Næstved; Study Chair: Sille Capion, MD, Lægehuset Ostenfeldt, Næstved; Study Chair: Rune F Nielsen, Nurse, Community Clinic Nakskov

Publications and helpful links

Helpful Links

• Open Science Framework platform for MOBILIZE
• MOBILIZE webpage

Study record dates

Study Major Dates

• Study Start (Actual): November 1, 2021
• Primary Completion (Estimated): July 31, 2024
• Study Completion (Estimated): July 31, 2024

Study Registration Dates

• First Submitted: November 2, 2020
• First Submitted That Met QC Criteria: November 19, 2020
• First Posted (Actual): November 27, 2020

Study Record Updates

• Last Update Posted (Actual): October 17, 2023
• Last Update Submitted That Met QC Criteria: October 13, 2023
• Last Verified: October 1, 2023

More Information

Terms related to this study

• Keywords: Exercise; Evaluation; Clinical Trial; Self-management; Multimorbidity
• Additional Relevant MeSH Terms: Pathologic Processes; Cardiovascular Diseases; Vascular Diseases; Respiratory Tract Diseases; Arteriosclerosis; Arterial Occlusive Diseases; Lung Diseases; Disease Attributes; Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases; Arthritis; Chronic Disease; Heart Diseases; Coronary Artery Disease; Myocardial Ischemia; Coronary Disease; Lung Diseases, Obstructive; Pulmonary Disease, Chronic Obstructive; Osteoarthritis; Osteoarthritis, Knee; Osteoarthritis, Hip
• Other Study ID Numbers: SJ-857; 801790 (Other Grant/Funding Number: European Research Council under the EU Horizon 2020 program)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: Data will be made available upon reasonable request after the primary publications have been published.
• IPD Sharing Time Frame: Ultimo 2024.
• IPD Sharing Access Criteria: Data will be made available upon reasonable request after the primary publications have been published.
• IPD Sharing Supporting Information Type: STUDY_PROTOCOL; SAP; ICF; ANALYTIC_CODE

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No