Group Lifestyle Balance Adapted for Individuals With Impaired Mobility (GLB-AIM) (GLB-AIM)
Mobility Limitation
About this trial
This is an interventional treatment trial for Mobility Limitation
Eligibility Criteria
Inclusion Criteria:
- being over 18 years old,
- having a permanent mobility impairment for at least 1 year,
- being overweight as evidenced by BMI > 25 or the equivalent value recommended for spinal cord injury and amputee populations,
- having sufficient upper arm mobility to engage in exercise, having access to a telephone, and
- obtaining physician signed clearance to participate in the weight management intervention.
Exclusion Criteria:
- disabilities for which cognitive impairment substantially impairs autonomy (e.g. mental retardation), as determined by a 5-item everyday autonomy scale,
- medical issues for which exercise is contraindicated such as uncontrolled hypertension or coronary heart disease,
- age 75 or older,
- pregnancy, and
- not fluent in English language.
The upper age cut off is intended to ensure that the sample consists of a population whose permanent mobility impairment is unrelated to aging. Pregnancy is excluded because it is directly related to weight gain.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
GLB-AIM
wait-list control
GLB-AIM (Group Lifestyle Balance program, Adapted for individuals with Impaired Mobility) is a 12-month intervention that promotes 5% weight loss by reducing calories and increasing exercise (150 minutes of moderate physical activity). The 23 GLB-AIM sessions were delivered through monthly in-person and teleconference calls and participants were encouraged to self-monitor daily caloric/fat intake and physical activity using materials to accurately measure daily calories and exercise, which included a food scale, measuring cups and spoons and a loaned Garmin vívofit® activity tracker and heart rate monitor. Participants shared their logs with lifestyle coaches over the 13 core sessions and lifestyle coaches provided positive reinforcement, feedback, and problem solving techniques as needed.
During the initial 6 month intervention period the control group received several contacts from the study staff via mail that included information on general health (e.g., managing stress, getting good sleep), holiday cards, and scheduling reminders for the 3 and 6 month testing.