- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06124911
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:
- 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.
- 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
Status
Recruiting
Conditions
Intervention / Treatment
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:
- Ashleigh Keenan, MRes
- Phone Number: 01912274700
- Email: ashleigh.keenan@northumbria.ac.uk
-
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.
Sponsor
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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