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The Long-Term Effects of Resistance Training and Diet in Elderly Type 2 Diabetics

The Long-Term Effects of Resistance Training and Diet in Elderly Type 2 Diabetics

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622000640707
Acronym
LLL study
Enrollment
29
Registered
2022-05-02
Start date
1999-06-07
Completion date
2000-01-28
Last updated
2022-05-09

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

Conditions

None listed

Brief summary

Non-insulin-dependent diabetes mellitus (NIDDM) is a leading cause of mortality in the adult population and its prevalence is known to rise steadily with increasing age. The presence of obesity and low levels of physical activity are the major lifestyle determinants of NIDDM. Given that both are potentially modifiable, there is universal agreement that lifestyle strategies emphasising improved diet and increased physical activity play important roles not only in the primary prevention of diabetes, but also the secondary prevention of diabetic complications arising from poor glycaemic control. Unfortunately, traditional approaches combining endurance-type exercise with dietary modifications, may be compromised in elderly NIDDM patients because of age-associated declines in muscle strength and functional capacity. Resistance (weight) training may be a plausible exercise alternative for elderly NIDDM patients because of its known effects on muscle strength, size and function. However, the efficacy and feasibility of dynamic resistance training in elderly NIDDM patients is not known. We postulate that the combination of resistance exercise training with moderate energy restriction will counterbalance fat-free mass loss often seen with energy restriction alone and may have additive or synergistic benefits in the non-pharmaceutical management of glycaemic control, cardiovascular risk factors and general well-being of elderly NIDDM patients. The aim of this randomised controlled trial is to therefore examine the safety, feasibility and effects of high-intensity PRT combined with healthy eating to elicit moderate weight loss in glycaemic control and body composition in those with type 2 diabetes.

Interventions

This study is a two-arm, 12-month RCT which will consist of two phases involving older overweight and obese adults with type 2 diabetes. Specifically, the program is designed to investigate whether 6 months of high intensity progressive resistance training (PRT) within a supervised and structured setting combined with weight loss (WL) can reduce HbA1C, increase muscle strength and lean body mass and decrease fat mass in older overweight and obese adults with T2D compared to weight loss alone Fo

This study is a two-arm, 12-month RCT which will consist of two phases involving older overweight and obese adults with type 2 diabetes. Specifically, the program is designed to investigate whether 6 months of high intensity progressive resistance training (PRT) within a supervised and structured setting combined with weight loss (WL) can reduce HbA1C, increase muscle strength and lean body mass and decrease fat mass in older overweight and obese adults with T2D compared to weight loss alone Following baseline assessments, participants will be randomised (1:1) ratio to receive either PRT + WL or sham (flexibility) training + WL. An accredited Exercise Physiologist will prescribe and supervise the initial exercise program. Those participants allocated to PRT + WL for the first six-months will attend the exercise laboratory at Deakin University three non-consecutive days per week and perform an individually prescribed 45-60 minutes, high intensity (75-85% of their one repetition maximum strength) program consisting of free weights and weights machines (three sets of 8-10 repetitions, nine exercises). Following the 6-month supervised gym-based intervention, participants will be prescribed a home-based exercise program in which they will be provided with individual instructions and equipment (dumbbells and ankle weights). Participants will be asked to train three days per week at home and/or at a community or commercial leisure centre. To facilitate transition to the home-based intervention, participants in the PRT + WL group will perform the home-based PRT program within the structured and supervised gym setting for the final month of phase 1. The home-based exercises (duration: 45-60 minutes) will replace weights machines with dumbbells and ankle weights and participants will be requested to complete nine exercises (three sets of 8-10 repetitions) with aim to exercise at a moderate intensity (at least 60% of maximum). Participants will attend the gymnasium once per month to monitor technique and progression and complete weekly exercise diaries to monitor adherence. In addition, weekly phone calls (first month) and subsequent fortnightly calls will monitor adherence and enable participant questions and feedback. Home visits will be conducted in week one to ensure safety and provide additional weights to facilitate progression. All participants will also be placed on a healthy eating plan supplying less than or equal to 30% total energy from total fat (less than or equal to 10% saturated fat) with protein and carbohydrate being distributed for remaining energy. Individually prescribed by a dietitian, the healthy eating plan is designed to induce moderate weight loss (~0.25 kg per week) throughout phase 1. Interviews every two weeks by the dietitian and completion of a weekly checklist will be used to assess adherence. Changes in nutrient intake will be assessed via a 3-day food record conducted at 3 and 6 months. Nutrition information will be analysed using Foodworks nutrient analysis software (Xyris, Brisbane, Queensland, Australia). Following the first 6-month gym-based intervention, participants will not be required to adhere to the healthy eating (WL) plan and will not receive further dietary recommendations.

Sponsors

Baker Heart and Diabetes Institute
Lead SponsorOther

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Participants must have established T2D (greater than 6 months), being treated with diet or oral hypoglycaemic agent (excluding insulin), HbA1c range 7-10%, overweight or obese (BMI greater than 27 kg/m2 and less than or equal to 40 kg/m2), not participating in regular PRT and engaging in less than 150 minutes moderate or less than 60 minutes vigorous exercise/week (preceding 6 months), non-smoker and consuming less than 2 alcoholic drinks/day.

Exclusion criteria

Participants will be excluded if history/evidence of ischemic heart disease, systemic diseases, hypertension (>160/90mmHg), advanced diabetic neuropathy and/or retinopathy and conditions (severe orthopaedic, cardiovascular or respiratory) that prevent participation and those with absolute exercise contraindications (American College of Sports Medicine).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 11, 2026