Health Promotion and Wellness Program for Adults With Disabling Conditions

Stroke Clinical Trial

Official title:

Examining the Efficacy of a SystemCHANGE™ Weight Management Intervention in Stroke Survivors and Persons With Chronic Inflammatory Autoimmune/Immune-mediated Diseases

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01776034
• Other study ID #: 07-14-16 / 03-14-24
• Status: Completed
• Phase: N/A
• Start date: January 2013
• Est. completion date: December 2016

Study information

• Verified date: January 2022
• Source: Case Western Reserve University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to conduct a randomized controlled pilot study to examine the efficacy, feasibility and safety of the SystemCHANGE™(SC) health promotion and wellness program in adults with disabling conditions. Particularly, the study will focus on developing a program of research on adapting and testing SC weight management interventions in overweight and obese stroke survivors and persons with chronic inflammatory autoimmune/immune-mediated diseases, specifically those with multiple sclerosis (MS) and rheumatoid arthritis (RA).

Description:

Individuals with disabling conditions, such as stroke, multiple sclerosis, or rheumatoid arthritis, face many barriers to engaging in physical activity, healthy nutritional habits, and good sleep hygiene. This leads to weight gain, de-conditioning, and declines in upper- and lower- extremity function, which makes it even more difficult to engage in healthy behaviors, thereby perpetuating a cycle of functional decline. Developing an effective weight management intervention may be a strategy for disrupting this disabling cycle and reducing the impact of the disease. Fostering a positive social environment may help adults with disabling conditions overcome barriers to engaging in healthy behaviors. SystemCHANGE (SC) is a new behavior change program that uses approaches consistent with social ecological theories and process improvement techniques (i.e. changing the dynamics of a system or group) to increase social support in lifestyle behaviors that promote energy balance. SC focuses on redesigning the social environment using a series of trial-and-error "experiments", which is in contrast to cognitive-behavioral interventions that focus on changing a person's viewpoint of a situation and increasing motivation. In a SC intervention, individuals are taught a set of skills to assist them in incorporating habitual lifestyle behaviors into their daily systems so they succeed despite wavering motivation. The rationale for developing a weight management intervention for these patients is to slow disability progression and prevent secondary conditions.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 66
• Est. completion date: December 2016
• Est. primary completion date: December 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 75 Years

Eligibility

Inclusion Criteria Stroke:

• Physician-confirmed diagnosis of stroke (> 6 weeks)

• Body mass index between 23 to 45 kg/m2

• Age 30 to 75 years

Exclusion Criteria Stroke:

• Pregnant or plans to become pregnant in the next 6 months

• Current participation in a face-to-face weight management program

• Uncontrolled diabetes (hospitalization within the prior 6 months)

• Serious mental illness

• Thyroid and adrenal gland diseases

• Inability to walk 3 meters with or without a cane or walker

• Severe cardiopulmonary disease that limits engagement in physical activity (e.g., myocardial infarction, congestive heart failure, coronary artery bypass grafting or valve replacement during the past three months, serious cardiac arrhythmias, hypertrophic cardiomyopathy, severe aortic stenosis, and pulmonary embolus) or abnormal blood pressure or heart rate response after the 6-Minute Walking Test (e.g., a drop in systolic blood pressure of >10mmHg from baseline)

• Severe cognitive deficits (Screening questioanire called the Short Orientation Memory-Concentration < 12)

• Currently taking oral corticosteroids, antipsychotic (except for depression medication), or medications specifically for weight loss

• 3 or more falls in the past month

• Bulimia

• Unable to speak English over the phone

• Able to eat independently and is not on a special diet because of difficulty in swallowing

• Unstable weight (gained or lost >10lbs in the last two months)

Inclusion Criteria MS or RA:

• Physician-confirmed diagnosis of multiple sclerosis or rheumatoid arthritis

• Body mass index between 23 to 45 kg/m2

Exclusion Criteria MS or RA:

• Pregnant or plans to become pregnant in the next 6 months

• Current participation in a face-to-face weight management program

• Uncontrolled diabetes (hospitalization within the prior 6 months)

• Serious mental illness

• Inability to walk 3 meters with or without a cane or walker

• Severe cardiopulmonary disease that limits engagement in physical activity

• Severe cognitive deficits (Short Orientation Memory-Concentration < 12)

• Currently taking oral corticosteroids, antipsychotic (except for depression medication), or medications specifically for weight loss

• 3 or more falls in the past month

• Bulimia

• Unable to speak English

• Uncontrolled thyroid or adrenal disease (change in type and dosage of medication within the prior 3 months)

Related Conditions & MeSH terms

• Multiple Sclerosis
• Rheumatoid Arthritis
• Stroke

Intervention

Behavioral:
• SystemCHANGE Group Lifestyle counseling

• Phone Lifestyle Counseling

Locations

Country	Name	City	State
United States	Case Western Reserve University	Cleveland	Ohio

Sponsors (3)

Lead Sponsor	Collaborator
Case Western Reserve University	American Heart Association, National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes from baseline in body weight.	A digital scale will be used to measure Body weight.	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).
Secondary	Changes from baseline in cardiovascular risk biomarkers.	The Alere Cholestech LDX 1 Analyzer will be used to measure Triglycerides levels.	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).
Secondary	Changes from baseline in Walking Test.	A Six Minute Walking Test will be administered using standardized instructions and verbal cues	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).
Secondary	Changes from baseline in 1-minute sit to stand test	A 1-minute sit to stand test will be administered using standardized instructions and verbal cues	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).
Secondary	Changes from baseline Physical Activity	Physical Activity and Disability Survey-Revised will be administered to assess physical function. Higher scores on the Physical Activity and Disability Survey-Revised indicates increased physical activity levels. Score range: Not applicable.	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).
Secondary	Changes from baseline Self-efficacy for weight management	Weight Efficacy Lifestyle Questionnaire-Short Form (WEL-SF) will be administered. A higher score on the weight efficacy lifestyle questionnaire indicates more confidence to engage in a healthy behavior (possible score range for self-efficacy weight is 1 to 10)	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).
Secondary	Changes from baseline social support for physical activity from family	Social Support for Exercise Behavior scales will be administered. A higher score on social support scales indicates greater social support from family to engage in physical activity (possible score range is 1 to 5).	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).
Secondary	Changes from baseline in emotional well-being	Quality of Life in Neurological Disorders (Neuro-Qol) positive affect & wellbeing questionnaires will be administered. Higher scores on Quality of Life in Neurological Disorders (Neuro-Qol) positive affect and well-being indicates a greater life satisfaction (possible score range 9 to 45).	Each patient will be given the assessments at 2 points during the study, at baseline and at posttest (an average of 6 months from baseline).