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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06124911
Enrollment
38
Registered
2023-11-09
Start date
2023-05-30
Completion date
2024-06-05
Last updated
2025-05-23

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

Conditions

Quality of Life

Keywords

Activities of Daily Living, Balance, Independence, Mobility, Untrained

Brief summary

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.

Interventions

OTHERLeg Press Resistance Training (3x5)

Leg Press resistance training at 60% one-rep-max for three sets of five repetitions

OTHERLeg Press Resistance Training (5x5)

Leg Press resistance training at 60% one-rep-max for five sets of five repetitions

Sponsors

Northumbria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 85 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Quality-of-lifeAt 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)

Secondary

MeasureTime frameDescription
6-minute Walk TestAt 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.
Timed-up-and-goAt 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.
30-second sit-to-stand (30s-Sit-to-Stand)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.
BalanceAt 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.
Body Mass IndexAt 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
Strength-to-mass RatioAt 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.
Leg press one-rep-max velocity pre-to-postAt 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.
StrengthAt 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.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026