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
1 other identifier
interventional
60
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 17, 2024
CompletedFirst Posted
Study publicly available on registry
December 31, 2024
CompletedStudy Start
First participant enrolled
January 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2025
CompletedFebruary 14, 2025
December 1, 2024
5 months
December 17, 2024
February 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Physical work capacity
A 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.
From enrollment to the end of study at 8 weeks
Secondary Outcomes (3)
Muscular Strength
From enrollment to the end of study at 8 weeks
BMI
From enrollment to the end of study at 8 weeks
Body Fat
From enrollment to the end of study at 8 weeks
Study Arms (2)
Control
NO INTERVENTION30 participants will be randomised into the CONTROL group and will continue to perform their normal activities. They will only be required to keep a log of their exercise intensity for each week over the 4-week period and record them on an online diary. The exercise log/diary consists of type of exercise, e.g. resistance or aerobic and duration of exercise session.
ROPES
EXPERIMENTALThe intervention is a 4-week training exercise program conducted by trained Physiotherapists.
Interventions
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.
Eligibility Criteria
You may qualify if:
- 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)
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Singapore General Hospital
Singapore, Singapore
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Principal Physiotherapist
Study Record Dates
First Submitted
December 17, 2024
First Posted
December 31, 2024
Study Start
January 2, 2025
Primary Completion
June 1, 2025
Study Completion
August 1, 2025
Last Updated
February 14, 2025
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share