Immediate, Residual, and Cumulative Effects of Fartlek, Hill Circuit, and Roll-On Training in Long-Distance Runners

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18-25
SponsorDebre Markos University

About this trial

This randomized controlled trial will compare Fartlek, hill circuit, and roll-on training in well-trained long-distance runners. Twenty-one eligible runners will be randomly assigned to one of three training groups and will complete a 12-week intervention comprising 24 prescribed training sessions. The study will evaluate immediate responses to conditioning, 24-hour recovery responses, and cumulative changes in running performance, aerobic fitness, and training-related responses. Outcomes will include heart rate, blood lactate concentration, rating of perceived exertion, delayed-onset muscle soreness, recovery and wellness indicators, internal training load, 5-km time-trial performance, and VO₂max. The findings will provide evidence regarding the comparative responses to these three conditioning modalities in well-trained long-distance runners.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Fartlek training

    Behavioral

    A structured variable-intensity running intervention administered for 12 weeks to trained long-distance runners. Each prescribed session includes standardized warm-up and cool-down periods, alternating faster and slower running at prescribed intensities, and prescribed recovery periods. Running duration, intensity, repetitions, recovery intervals, and workload progression are standardized according to the study protocol. Training sessions are supervised, and exercise intensity is monitored using heart rate, rating of perceived exertion, running pace, and prescribed workload.

  • Hill Circuit

    Behavioral

    A structured hill-running and circuit-based training intervention administered for 12 weeks to trained long-distance runners. Each prescribed session includes standardized warm-up and cool-down periods, repeated uphill running bouts, running-based circuit exercises, and prescribed recovery intervals. Hill gradient, running duration, repetitions, exercise intensity, recovery intervals, and workload progression are standardized according to the study protocol. Exercise intensity is monitored using heart rate, rating of perceived exertion, running pace, and prescribed workload.

  • Roll-On

    Behavioral

    A structured progressive running intervention administered for 12 weeks to trained long-distance runners. Each prescribed session includes standardized warm-up and cool-down periods, controlled running with planned gradual increases and decreases in running speed, and prescribed recovery periods where applicable. Running duration, speed progression, intensity, repetitions, recovery intervals, and workload progression are standardized according to the study protocol. Exercise intensity is monitored using heart rate, rating of perceived exertion, running pace, and prescribed workload.

Treatment groups

21 Participants
are divided into 3 treatment groups
Group A: Fartlek Training Group (FTG)Experimental treatment 1 intervention
Group B: Hill Circuit Training Group (HCTG)Experimental treatment 1 intervention
Group C: Roll-On Training Group (ROTG)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

5-km Time-Trial Performance

Change in 5-km time-trial completion time from baseline to Week 6 and Week 12, comparing the Fartlek Training Group (FTG), Hill Circuit Training Group (HCTG), and Roll-On Training Group (ROTG).

Time frame
Baseline week 6 and Week 12

Secondary outcomes

1

VO₂max

Change in maximal oxygen uptake (VO₂max), measured in mL/kg/min, from baseline to Week 6 and Week 12, comparing FTG, HCTG, and ROTG.

Time frame
Baseline, Week 6, and Week 12
2

Blood Lactate Concentration

Change in blood lactate concentration, measured in mmol/L, immediately following prescribed conditioning sessions to characterize the acute physiological response to Fartlek, Hill Circuit, and Roll-On training.

Time frame
Immediately pre-training and post-training during intervention sessions in Weeks 1-12
3

Rating of Perceived Exertion (RPE)

Session rating of perceived exertion will be measured using the OMNI perceived-exertion scale immediately following each conditioning session.

Time frame
Immediately after each training session during Weeks 1-12
4

Heart Rate Response

Change in average and maximum heart rate during prescribed conditioning sessions to characterize the acute cardiovascular response to Fartlek, Hill Circuit, and Roll-On training.

Time frame
During each training session during Weeks 1-12

Other outcomes

1

Delayed-Onset Muscle Soreness (DOMS)

Change in self-reported muscle soreness following each prescribed conditioning session to assess post-exercise muscular recovery.

Time frame
Immediately post-training and 24 hours after each conditioning session during Weeks 1-12
2

Recovery and Wellness

Change in recovery and wellness indicators, including sleep duration, sleep quality, fatigue, stress, mood, and overall wellness score, assessed following conditioning sessions.

Time frame
Before and 24 hours after each conditioning session during Weeks 1-12
3

Acute Training Load

Weekly acute internal training load calculated from accumulated session training loads, where session training load is calculated as session duration multiplied by session rating of perceived exertion (sRPE).

Time frame
Weeks 1-12
4

Chronic Training Load

Chronic internal training load calculated as the rolling 4-week average of weekly training load during the intervention.

Time frame
Weeks 4-12

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Debre Markos University

Lead sponsor

Bahir Dar University

Collaborator

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