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Rapid Optimisation of Performance Enhancement and Skill (ROPES)

The Effectiveness of Rapid Optimisation of Performance Enhancement and Skill (ROPES) as an Exercise Training Programme for Sedentary Health Care Staff

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06754007
Enrollment
60
Registered
2024-12-31
Start date
2025-01-02
Completion date
2025-08-31
Last updated
2025-02-14

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

Conditions

Sedentary Lifestyle

Keywords

Sedentary, healthcare workers

Brief summary

Despite innate knowledge of the benefits of regular physical activity, healthcare workers are just as physically inactive as the general population. Physical activity interventions delivered at the workplace seem perfect to improve the health of this large population. The aim of the study is to deliver an efficacious, minimal time impost training program targeted at optimising health benefit while overcoming time-related barriers to initial uptake of regular exercise.

Detailed description

To evaluate the effectiveness of a 4-week, easily accessible, time-optimised exercise program (ROPES - Rapid Optimisation of Performance Enhancement and Skill) for healthcare workers. 60 staff recruited from Singapore General Hospital (SGH) will be randomly assigned into 2 groups, CONTROL or ROPES group. The ratio to intervention and control group is at 1:1. The staff will be assigned to each group respectively.

Interventions

PROCEDUREROPES Training Programme

ROPES is a training programme that involves resistance training, whole-body exercises and HIIT aerobic sessions with each session lasting no longer than 45 minutes.

Sponsors

Singapore General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age group: 21 - 70 years old * All participants must be free of musculoskeletal, surgical and/or neurological injury in the past 6 months. * Participants not engaged actively in regular exercise i.e. exercises less than once a week and at a duration less than 30 mins per session. * Healthy with stable management of any existing diabetes, cholesterol and/or hypertension. * They should have no issues with the Physical Activity Readiness Questionnaire (PAR-Q)

Exclusion criteria

* Participants under the age of 21 or over the age of 70 * Newly diagnosed diabetes/metabolic syndrome/high cholesterol or uncontrolled high BP \>160 mmHg and under medical supervision. * Subjects with cardiovascular conditions and on beta-blockers. * Subjects who are pregnant or with recent (\< 3 months) diagnosis of a medical condition, especially cardiac-related conditions.

Design outcomes

Primary

MeasureTime frameDescription
Physical work capacityFrom enrollment to the end of study at 8 weeksA standard physical work capacity test based on the linear relationship between heart rate, power output and oxygen consumption will estimate the work capacity. The higher the heart rate, the better the physical work capacity. Minimum value of heart rate is 155 bpm and maximum value is 199 bpm.

Secondary

MeasureTime frameDescription
Muscular StrengthFrom enrollment to the end of study at 8 weeksHandgrip strength will be measured using a hand-held dynamometer to determine functional strength.
BMIFrom enrollment to the end of study at 8 weeksHeight and weight will be measured on a body fat analyser and will be combined to report the BMI in kg/m\^2.
Body FatFrom enrollment to the end of study at 8 weeksBody fat will be measured on a body composition analyser and will be reported in percentage %.

Countries

Singapore

Contacts

Primary ContactCelia Ia Choo Tan, PhD (Dept of Surgery)
celia.tan.i.c@singhealth.com.sg+65 63265281

Outcome results

None listed

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