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Lifestyle Intervention Trial in Obese Elderly

Exercise Interventions During Voluntary Weight Loss in Obese Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01065636
Acronym
LITOE
Enrollment
160
Registered
2010-02-09
Start date
2010-02-28
Completion date
2018-12-31
Last updated
2020-01-22

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

Conditions

Obesity

Brief summary

Obesity causes frailty in obese older adults by exacerbating the age-related decline in physical function. However, appropriate management of obesity in older adults is controversial. Weight loss without exercise could worsen frailty by accelerating the usual age-related decline in muscle and bone mass that leads to sarcopenia and osteopenia, respectively. Because of the important problem of frailty in obese older adults, it is important to determine the most efficacious approach in reducing, or even reversing frailty in this population. The primary objective of this proposal is to evaluate which distinct type of physical exercise (resistance, aerobic, or combined resistance + aerobic) is most efficacious in preventing the weight-loss-induced reduction in muscle and bone mass and reversing frailty in obese older adults.

Interventions

BEHAVIORALDiet + Resistance Training

Behavioral Therapy through a lifestyle modification program, Diet therapy once weekly through a dietician prescribed diet for 26 weeks, and resistance exercise training 3-days/week for 24 weeks.

BEHAVIORALDiet + Aerobic Training

Behavioral Therapy through a lifestyle modification program, Diet therapy once weekly through a dietician prescribed diet for 26 weeks, and aerobic exercise training 3-days/week for 24 weeks

BEHAVIORALDiet + Resistance/Aerobic Exercise

Behavioral Therapy through a lifestyle modification program, Diet therapy once weekly through a dietician prescribed diet for 26 weeks, and combined resistance/aerobic exercise training 3-days/week for 24 weeks

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
Baylor College of Medicine
CollaboratorOTHER
Biomedical Research Institute of New Mexico
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
65 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* 65-85 years old * Obese men and women (BMI \> or equal to 30 kg/m2) * Stable weight (±2 kg) during the last 6 mos. * Must be sedentary (regular exercise \<1 h/wk or \<2 x/wk for the last 6 mos.) * Be judged, during the initial screening, to be well motivated and reliable

Exclusion criteria

* Any major chronic diseases * Any condition or unstable diseases that would interfere with exercise or dietary restriction, in which exercise or dietary restriction are contraindicated, or that would interfere with interpretation of results that include but are not limited to: * Cardiopulmonary disease (e.g., recent MI, unstable angina, stroke etc.) * Severe orthopedic/musculoskeletal or neuromuscular impairments that would contraindicate participation in exercise * Visual or hearing impairments that interfere with following directions * Diagnosis of dementia * History of malignancy during the past 5 yr * Recent use of bone acting drugs (e.g. use of estrogen, or androgen containing compound, raloxifene, calcitonin, parathyroid hormone during the past year or biphosphonates during the last two years) * Individuals on insulin or with a fasting blood glucose of \> 140mg/dl, and/or a 2 hour post-glucose of \>250 mg/dl * BMD t-scores of \<-2.3 of the lumbar spine and proximal femur * serum creatinine \>2.0 mg/dl * No commitments, life situations or conditions that would interfere with their participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Change in Physical Function6 MonthsThe Physical Performance Test includes seven standardized tasks (walking 15.2 m \[50 ft\], putting on and removing a coat, picking up a penny, standing up from a chair, lifting a book, climbing one flight of stairs, and performing a progressive Romberg test) plus two additional tasks (going up and down four flights of stairs and making a 360-degree turn). The score for each task ranges from 0 to 4, with higher scores indicating better physical performance; a perfect score would be 36.

Secondary

MeasureTime frameDescription
Change in areal bone mineral density6 monthsAssessed by using DXA
Change in systolic and diastolic blood pressure6 monthsAssessed by using sphygmomanometer
Change in serum glucose6 monthsAssessed by glucose oxidase method
Change in serum lipids6 monthsAssessed by automated enzymatic/colorimetric assays
Change in biochemical marker for bone turnover and bone metabolism6 monthsAssessed by using enzyme linked immunoabsorbent assay and radioimmunoassay
Change in circulating cytokines6 monthsAssessed by using enzyme linked immunoassay
Change in adipocytokines6 monthsAssessed by using enzyme linked immunoassay
Change in aerobic capacity6 monthsAssessed by using indirect calorimetry during graded exercise stress test
Change in fat mass6 monthsAssessed using DXA
Change in muscle strength6 monthsAssessed using 1-repetition maximum and dynamometry
Change in lean mass6 monthsAssessed using dual energy x-ray absorptiometry (DXA)
Change in habitual physical activity assessed by questionnaires6 monthsUsing the Stanford physical activity questionnaire (score range: 0 to 40 with higher scores indicating higher physical activity levels)
Change in habitual physical activity measured objectively6 monthsUsing accelerometers
Change in serum insulin6 monthsAssessed by immunoassay
Change in serum estradiol6 monthsAssessed by immunoassay
Change in 25 hydroxyvitamin D6 monthsAssessed by immunoassay
Change in Impact of Weight on Quality of Life_Lite (IWQOL-lite) score6 monthsAssessed by IWQO-liteL questionnaire
Change in Medical Outcomes 36-Item short form Health survey (SF-36)6 monthsAssessed by Physical component summary and mental component summary score (score range 0 to 100, with higher scores indicating better health status)
Change in gait speed6 monthsMeasured as time to walk a certain distance
Change in protein expression of muscle anabolic and catabolic factors6 monthsAssessed by western blotting
Change in concentration of targeted metabolites6 monthsAssessed by liquid chromatography hyphenated with mass spectrometry techniques
Change in dynamic balance6 monthsAssessed by the obstacle course
Change in static balance6 monthsAssessed by one leg stance
Change in modified mini-mental exam6 monthsAssessed by using cognitive instrument testing
Change in word fluency6 monthsAssessed by using cognitive instrument testing
Change in trail a and trail b6 monthsAssessed by using cognitive instrument testing
Change in Ray Auditory verbal learning test6 monthsAssessed by using cognitive instrument testing
Change in muscle protein synthesis rate6 monthsAssessed by stable isotope methodology
Change in thigh muscle and fat mass6 monthsAssessed by magnetic resonance imaging (MRI)
Change in visceral fat mass6 monthsAssessed by MRI
Change in mood6 monthsAssessed by geriatric depression scale (score range: 0 to 30, where lower scores indicating better mood)
Change in waist circumference6 monthsUsing a tape measure
Change in serum testosterone6 monthsAssessed by immunoassay
Change in subjective ability to function6 monthsAssessed by Functional Status Questionnaire (score range: 0 to 36 with higher scores indicating better function)
Change is serum sclerostin6 monthsAssessed by immunoassay
Change in parathyroid hormone6 monthsAssessed by immunoassay
Change in gene expression of muscle anabolic and catabolic factors6 monthsAssessed by reverse transcription polymerase chain reaction and nanostring

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026