Low-dose Maximal-intent Versus Controlled-tempo Resistance Training on Quality-of-life in Older Adults

November 6, 2023 updated by: Northumbria University

Comparison of Two Low-dose Resistance Training Modalities on Strength, Functional Capacity, and Quality-of-life in Healthy, Community-dwelling, Untrained Older Adults: a Randomised Controlled Trial

The aims of this study were to:

  1. Compare the effects of low-dose Maximal Intent and Controlled Tempo Resistance Training on untrained healthy older adults' quality-of-life, functional capacity, and strength.
  2. Qualitatively explore perceptions of Maximal Intent and Controlled Tempo Resistance Training in older adults.

Older adults are defined as being 60 or more years of age.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Tyne And Wear
      • Newcastle, Tyne And Wear, United Kingdom, NE1 8ST
        • Recruiting
        • Northumbria University
        • Sub-Investigator:
          • Gill Barry, PhD
        • Sub-Investigator:
          • Stuart Goodall, PhD
        • Contact:
        • Sub-Investigator:
          • Kai T Fox, MRes
        • Sub-Investigator:
          • Ashleigh Keenan, MRes
        • Sub-Investigator:
          • David G Behm, PhD
        • Sub-Investigator:
          • Sam Stuart, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Participants were eligible if they were between 30-60 years old
  • Uninjured
  • Had no cardiovascular or neuromuscular conditions
  • Had not participated in lower-limb resistance training in the previous six months.

Exclusion Criteria:

  • Participants were excluded if they had either taken part in any lower-limb resistance training in the last six months
  • Had underlying health condition(s) that prevented them from participating in resistance training
  • Regularly met or exceeded the UK recommended physical activity guideline of 150-minutes of moderate to intense physical activity per week.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Maximal-intent Resistance Training - 3x5 (MI3x5)
The max-intent group were instructed and encouraged to deliberately commit to exerting maximal effort and force during the concentric phase of the leg press with the intention of achieving the greatest velocity possible. This group completed 3 sets of 5 repetitions at 60% one-repetition maximum.
Leg Press resistance training at 60% one-rep-max for three sets of five repetitions
Experimental: Maximal-intent Resistance Training - 5x5 (MI5x5)
The max-intent group were instructed and encouraged to deliberately commit to exerting maximal effort and force during the concentric phase of the leg press with the intention of achieving the greatest velocity possible. This group completed 5 sets of 5 repetitions at 60% one-repetition maximum.
Leg Press resistance training at 60% one-rep-max for five sets of five repetitions
Experimental: Controlled-tempo Resistance Training - 3x5 (CT3x5)
The controlled-tempo group followed a metronome for both eccentric and concentric phases of the leg press with the intention of maintaining a steady three-second concentric and three-second eccentric. This group completed 3 sets of 5 repetitions at 60% one-repetition maximum.
Leg Press resistance training at 60% one-rep-max for three sets of five repetitions
Experimental: Controlled-tempo Resistance Training - 5x5 (CT5x5)
The controlled-tempo group followed a metronome for both eccentric and concentric phases of the leg press with the intention of maintaining a steady three-second concentric and three-second eccentric. This group completed 5 sets of 5 repetitions at 60% one-repetition maximum.
Leg Press resistance training at 60% one-rep-max for five sets of five repetitions

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality-of-life
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Participant quality of life (measured through focus group questions & SF-36)
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Balance
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Using the biodex to do a 3 x 20s double-foot eyes-open balance test on Level 6.
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
6-minute Walk Test
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
A "brisk"-paced 6-minute walk test.
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Timed-up-and-go
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Standing from a chair, walking to a point 3 metres away, turn, and return to the chair as quick as possible whilst walking.
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
30-second sit-to-stand (30s-Sit-to-Stand)
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Maximal amount of repetitions a participant can stand up from a chair in 30-seconds.
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Strength
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Participants one-repetition max on leg press machine.
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Body Mass Index
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Mass and height will be combined to report BMI in kg/m^2
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Strength-to-mass Ratio
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Mass and Leg Press 1RM will be combined to calculate strength-to-mass ratio.
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Leg press one-rep-max velocity pre-to-post
Time Frame: At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.
Velocity (m/s) of leg press measured at post-intervention, using baseline one-rep-max.
At baseline and Week 1, mid (Week 4), and post (Week 9), out of a total study duration of 9 weeks.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 30, 2023

Primary Completion (Estimated)

September 30, 2024

Study Completion (Estimated)

September 30, 2024

Study Registration Dates

First Submitted

October 29, 2023

First Submitted That Met QC Criteria

November 6, 2023

First Posted (Actual)

November 9, 2023

Study Record Updates

Last Update Posted (Actual)

November 9, 2023

Last Update Submitted That Met QC Criteria

November 6, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • NU2863

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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