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Group Lifestyle Balance Adapted for Individuals With Impaired Mobility (GLB-AIM)

Group Lifestyle Balance Adapted for Impaired Mobility (GLB-AIM): Translating the GLB to Promote Healthy Weight in People With Mobility Disability (Impairment)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03307187
Acronym
GLB-AIM
Enrollment
67
Registered
2017-10-11
Start date
2015-05-01
Completion date
2017-02-01
Last updated
2026-02-12

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

Conditions

Mobility Limitation

Brief summary

This study tested the effectiveness of the Group Lifestyle Balance™ (GLB) program adapted specifically for people with impaired mobility using standard behavioral approaches for weight loss. The overarching aim of this study was to promote health and reduce chronic disease risk among people with mobility impairment by building an evidence base for weight loss. The central hypothesis was that participants randomized to the intervention arm of the adapted GLB would show significant improvements on primary outcomes of weight and PA compared to a 6-month wait-list control group at 3 and 6 months, and show improvements on several secondary health outcomes.

Detailed description

The following are the specific study aims and hypotheses: Aim 1: To create an appropriate and usable adaptation of the GLB program for people with mobility impairment. Hypothesis 1.1: Advisory board participants will identify key adaptations to make the GLB materials appropriate and usable for individuals with impaired mobility. Aim 2: To establish whether the adapted GLB program for people with mobility impairment is a feasible intervention. Hypothesis 2.1: Intervention participants will rate the program satisfactorily and attend at least 2/3rd of the weekly group-based meetings and monthly individualized phone calls. Lifestyle coaches will also rate the adapted program satisfactorily. Aim 3: To determine if the GLB intervention adapted for those with mobility impairment is effective as determined by significant improvement in the primary and secondary outcomes in the intervention group compared to the wait-list control group at 3 and 6 months from baseline. Hypothesis 3.1: The intervention group will demonstrate significantly greater improvements in our primary outcomes (weight and PA) than the wait list control group at 3 and at 6 months and will show significant improvements in secondary outcomes at 6 months. Hypothesis 3.2: Both groups combined will demonstrate significantly greater improvements in the primary outcomes (weight and PA) after 3, 6 and 12 months of intervention and secondary outcomes after 6 and 12 months of intervention.

Interventions

BEHAVIORALGLB Adapted for Individuals with Impaired Mobility

The 12-month Group Lifestyle Balance program, Adapted for individuals with Impaired Mobility (GLB-AIM) promotes 5% - 7% weight loss by reducing calories and increasing energy expenditure to 150 minutes of weekly activity. The 23 GLB-AIM sessions were delivered through monthly in-person and teleconference calls. 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.

Sponsors

Baylor Research Institute
Lead SponsorOTHER
Centers for Disease Control and Prevention
CollaboratorFED

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 74 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
weight change12 monthschange in weight collected on 4 times over the year. Weight was measured using a Seca accessible scale (#676); wheelchair users were weighed in their chair on the scale, then transferred to a PT mat table from their chair scale to have their chair weighted separately and body weight was calculated as wheelchair weight subtracted from total weight.

Secondary

MeasureTime frameDescription
Session Attendance12 monthsSession attendance recorded for each of the 23 sessions and reported as average attendance at each session
self-monitoringover 13 core weeksself-monitoring adherence for daily food intake
physical activitybaseline, 3, 6, and 12 monthsself reported physical activity reported on the brief International Physical Activity Questionaire as minutes per week spent in moderate-intensity activity, vigorous-intensity activity, moderate and vigorous activity combined, and minutes per week walking/wheeling
waist circumferencebaseline, 6, and 12 monthswaist circumference measured while participants laid supine on a PT mat table at the level of the umbilicus, using a fabric measuring tape.
hemoglobin A1cbaseline, 6, and 12 monthshemoglobin A1c was collected by blood draw and sent to the lab for analysis
blood pressurebaseline, 6, and 12 monthsresting blood pressure after sitting quietly for 10 minutes using an Omron 3 Series wrist worm blood pressure cuff
cholesterolbaseline, 3, 6, and 12 monthstotal cholesterol was collected by blood draw during the non-fasting state and sent to the lab for analysis
self-efficacybaseline, 3, 6, and 12 monthsself-efficacy for health promoting behaviors: 27-items of the Self-Rated Abilities for Health Practices scale which assesses participants perceived ability to engage in health promoting activities across 4 domains (Nutrition, Exercise, Health Practices, Psychological Well Being, plus a total self-efficacy score)

Contacts

PRINCIPAL_INVESTIGATORKatherine Froehlich Grobe, PhD

Baylor Institute for Rehabilitation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026