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The objectives of the study are comparing the risk of injury and the running performance among novice runners with two different training programmes. The first programme has less running volume but more strengthening than the second one which is a normal running programme with no specific strengthening program.
This study will provide necessary information for a multicentric study to come. The information needed for this bigger study are the sample size, the attrition rate, the drop-out rate and the feasibility of the timeline.
The objectives of the study are comparing the risk of injury and the running performance among novice runners with two different training programmes. The first programme has less running volume but more strengthening than the second one which is a normal running programme with no specific strengthening program.
Hypothesis: A training programme with less running but strengthening exercises based on interval technique and strength could have similar or better results regarding running related injuries and performance compared to a normal training programme.
The experimentation will take place in Louvain-la-Neuve in Belgium. Most of the common trainings will take place on the 400m outdoor track field of of the University. A sample of local university students will be drawned. The sex proportion of the participants should be representative of the population (non-runners population), thus 50/50. They will have to be non-runners in good and healthy condition. A non-runner is defined as someone who did not practice regular running at least twice a week for the last 6 months and could not perform a 10km at enrolment.
50 participants will take part in this experimentation. They will be randomized into 2 groups of 25. The investifator hypothesize that 40 participants will follow the study until the end.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| strengthening running program | Experimental | The experimental group will undergo a specific running training based on leg strength training and interval running |
|
| Running program | Active Comparator | This running group will serve as control and will undergo a traditional running program composed of only running |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Strengthening | Other | The strengthening exercises were executed with the body weight without any additional weight and were composed of exercises like the squats, the lunges, the plank, and the mountain climbers |
| Measure | Description | Time Frame |
|---|---|---|
| Aerobic performance | aerobic performance testing using VAM-EVAL procedure | at baseline |
| Aerobic performance | aerobic performance testing using VAM-EVAL procedure | at 21 weeks of training |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of running related injuries | number of injuries due to running participation | from baseline to 21weeks, up to 21 weeks total |
| drop-out | abandon from the running program for any reason except running related injuries |
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Inclusion Criteria:
A novice runner was defined as someone who has not been running more than once a week for more than six months. The participants were systematically excluded if they did not match the interval of age, were not considered as novice runners, i.e., ran twice or more times a week for more than six months
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Irec/Nmsk | Brussels | 1200 | Belgium |
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| ID | Term |
|---|---|
| D055070 | Resistance Training |
| D012420 | Running |
| ID | Term |
|---|---|
| D005081 | Exercise Therapy |
| D012046 | Rehabilitation |
| D000359 | Aftercare |
| D003266 | Continuity of Patient Care |
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Randomised control trial (pilot study)
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The investigator were blinded for group distribution and randomisation. They also were the outcome assessor and were therefore kept blinded.
| Running | Other | running for two supervised training sessions of one hour, and one free session of 30 minutes per week during 24 weeks |
|
| from baseline to 21weeks, up to 21 weeks total |
| D005791 |
| Patient Care |
| D013812 | Therapeutics |
| D026741 | Physical Therapy Modalities |
| D064797 | Physical Conditioning, Human |
| D015444 | Exercise |
| D009043 | Motor Activity |
| D009068 | Movement |
| D009142 | Musculoskeletal Physiological Phenomena |
| D055687 | Musculoskeletal and Neural Physiological Phenomena |
| D008124 | Locomotion |