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Clinical Trials/NCT05885165
NCT05885165
Active, not recruiting
Not Applicable

Supervised Online Team-based Resistance Training Versus Unsupervised Self-administered Resistance Training for Elders: a Randomized Intervention Trial

University of Copenhagen1 site in 1 country70 target enrollmentFebruary 20, 2023
ConditionsHealthy Aging

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Aging
Sponsor
University of Copenhagen
Enrollment
70
Locations
1
Primary Endpoint
Change in 5 times sit-to-stand
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

The primary goal of this project is to investigate whether online supervised team-based exercise training is superior for increasing functional strength in elders compared to prescribed self-administered exercise training. Secondarily, the project aims to investigate whether adherence to online supervised team-based exercise training is greater compared to prescribed self-administered training, and if online supervised team-based exercise training can increase quality of life. Finally, this project will generate more knowledge on elderly individuals' approaches and responses to physical exercise through online services. The participants will undergo a 12-week intervention where they will be performing prescribed physical exercise for 5 hours bi-weekly and complete a 3-day dietary registration three times during the study. Participants will be randomized (2:1 ratio) to two groups and will: i) undergo supervised training in groups on an online live meeting platform by trained personnel, or ii) receive prescribed exercises through an online exercise platform but their training will be self-administered and unsupervised.

Registry
clinicaltrials.gov
Start Date
February 20, 2023
End Date
November 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Faidon Magkos

Professor

University of Copenhagen

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 65 years.
  • Danish reading and listening proficiency.
  • Participant is in possession of either a computer, tablet, or smartphone in order to participate in Zoom meetings (supervised team-based group) or training programs via Exorlive (unsupervised group).
  • The participant is able to walk independently and without external aids.

Exclusion Criteria

  • BMI \> 35 kg/m
  • Participation in other intervention studies or intention to do so, which are likely to affect the present study.
  • Known diseases which may affect energy expenditure and/or satiation/satiety/food intake i.e. inflammatory bowel disease, thyroid diseases.
  • Current diagnosis of eating disorder (e.g. restrained eating, disinhibition, emotional eating).
  • Psychiatric disorders i.e. schizophrenia, bipolar disease or depression with hospitalization within the last 6 months.
  • History or diagnosis of cardiovascular disease including current angina; myocardial infarction; coronary revascularization procedures; stroke (either ischemic or hemorrhagic, including transient ischemic attacks); symptomatic peripheral artery disease that required surgery or was diagnosed with vascular imaging techniques; ventricular arrhythmia; uncontrolled atrial fibrillation; congestive heart failure (New York Heart Association Class II to IV); myocardiopathy; and history of aortic aneurysm ≥5.5 cm in diameter or aortic aneurysm surgery within the past six months, as diagnosed by a medical doctor.
  • Systolic blood pressure above 160 mmHg and/or diastolic blood pressure above 100 mmHg whether on or off treatment for hypertension. If being treated, stable treatment (i.e. no change in treatment, either dose, type of medication or other changes) within the last three months is required.
  • History or diagnosis of chronic kidney disease.
  • History or diagnosis of liver disease.
  • Active inflammatory bowel disease, celiac disease, chronic pancreatitis or other disorder potentially causing malabsorption.

Outcomes

Primary Outcomes

Change in 5 times sit-to-stand

Time Frame: Week 0 and week 13

Physical function, assessed by the '5 times sit-to-stand' (5xsts) test

Secondary Outcomes

  • Change in 1 repetition maximum (RM) leg press(Week 0 and week 13)
  • Change in Fat mass(Week 0 and week 13)
  • Change in Fat-free mass(Week 0 and week 13)
  • Change in Resting blood pressure(Week 0 and week 13)
  • Change in Quality of life (RAND 36-item health survey)(Week 0 and week 13)
  • Change in Aerobic fitness(Week 0 and week 13)
  • Change in Balance(Week 0 and week 13)
  • Adherence to exercise(At every training from week 1-12)
  • Food records(Week 1, Week 6, and Week 12)

Study Sites (1)

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