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Healthy WomenNCT05777265

The Effects of 16-Week Circuit Training in Healthy Women

A study testing Circuit Training in people with Healthy Women, run by Manisa Celal Bayar University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of this study is to investigate the effects of 16-week CT on physical fitness parameters, pulmonary function, and quality of life in healthy women. Read more about this study

Who is it for?
Ages 18 to 45 years, women onlyHealthy volunteers can take part
Conditions the study is for
Healthy Women
What is being tested?
Circuit Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
29 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Mar 2023to 15 Jul 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • volunteering to participate in study
  • not have any musculoskeletal disease

Who cannot join

  • history of malignancy
  • using any drugs or supplement
  • history of any surgery
  • being pregnant

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • İzmir Katip Celebi University

    Izmir

Other trials in Turkey (Türkiye)

About this study

Official title: The Effects of 16-Week Circuit Training on Physical Fitness Parameters, Pulmonary Function, and Quality of Life in Healthy Women

The aim of this study is to investigate the effects of 16-week CT on physical fitness parameters, pulmonary function, and quality of life in healthy women.

Read the detailed description

Circuit training (CT) is an important type of training that can combine different types of exercises in a single form of training. This training is generally circular with the different exercise stations it contains, so it is known as CT. The initial protocol of this training, developed by researchers at the University of Leeds in 1953, consisted of 9 to 12 moderate intensity exercises (40% to 60% of 1RM) performed at different exercise stations and with a specific repetition and duration. Nowadays, it is seen that this training is applied in different intensities and protocols. Also, CT has gained popularity due to its practicality and effectiveness and is preferred by all age groups in recent years.

CT can be applied in many sport settings and does not require expensive equipment. Also, this training can be adjusted to any level of physical fitness and includes bodyweight exercises and functional movements. This training generally includes aerobic and strengthening exercises and improves musculoskeletal, cardiovascular and pulmonary functions. On the other hand, CT allows individual interaction both between participants and between participants and the sports or health professionals who provide this training. Lastly, the hallmark of CT is that it includes different exercise stations and short rest periods without breaks and the advantage of CT is that it effectively improves several parameters of physical fitness simultaneously.

Current literature investigating the effects of CT on physical fitness parameters in different populations is still emerging. However, it was seen that few studies focused on the healthy women population. Also, it was concluded that these studies reported different results regarding the effects of CT. Accordingly, it has been concluded that 6-week CT improved lower and upper extremity muscle strength and endurance, but had no positive effect on flexibility and body composition in healthy women. However, it has been reported that 12-week CT had no positive effect on body composition, knee flexor and extensor muscle strength in healthy women. Lastly, it has been concluded that12-week of CT had positive effects on body composition, and improved flexibility and lower extremity muscle strength in healthy women. These results in the literature suggested there is no clear consensus on the effects of CT on physical fitness parameters in healthy women.

Moreover, the fact that CT also includes aerobic exercises shows this training may also have an effect on pulmonary function. In this context, previous studies reported the positive effects of this training on pulmonary function in adolescent, professional volleyball players, women with sarcopenia, and people with human immunodeficiency virus. However, there is insufficient evidence regarding the effects of CT on pulmonary function in healthy women. To the best of our knowledge, only one previous study reported the positive effects of CT on some pulmonary function in healthy women. Accordingly, it is clear that studies is needed to examine the effects of CT on pulmonary function on healthy women. This training may also improve pulmonary function in healthy women by increasing the performance of the diaphragm muscle through aerobic exercise. Moreover, these positive effects on pulmonary function may also improve quality of life in healthy women. Lastly, similar to physical fitness parameters, studies investigating the effects of CT on quality of life also included different populations. However, it was concluded there were few studies that included healthy women and the results of these studies differed.

Therefore, the aim of this study is to investigate the effects of 16-week CT on physical fitness parameters, pulmonary function, and quality of life in healthy women. Also, the investigators hypothesized that the 16-week CT would be positive effects on physical fitness parameters, pulmonary function, and quality of life in healthy women.

Conditions
Healthy Women
Being tested
Circuit Training
Keywords
Health, Exercise, Physical Fitness, Women
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Circuit TrainingOther

    CT will be applied to the participants, taking into account the recommendations of the American College of Sports Medicine (ACSM), 3 days a week, an average of 40 minutes a day, for a total of 16 weeks. Warm-up and cool-down protocols will be applied before and after each CT, and each exercise will be performed as 15 repetitions and an average of 40 seconds of rest will be given between exercises. Also, the intensity of CT will be determined according to the Borg scale (between 11 and 14). CT will include 'mini squat', 'step up', 'sit ups', 'reverse sit ups', 'leg press', 'leg curl', 'leg extension', 'crunches', 'lunge', 'prone bridge', and 'side bridge' exercises.

Study groups in NCT05777265
Study groupRoleWhat they receive
Training GroupExperimentalCT will be applied to the participants, taking into account the recommendations of the American College of Sports Medicine (ACSM), 3 days a week, an average of 40 minutes a day, for a total of 16 weeks
Receives: Other: Circuit Training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Body Mass Index (kg/m2)

    Body Mass Index (kg/m2) will be assessed with the Bioelectrical Impedance Analysis System.

    Measured: Sixteen week

  2. Waist(cm)/Hip(cm) Ratio (%)

    Waist(cm)/Hip(cm) Ratio (%) will be assessed with the Bioelectrical Impedance Analysis System.

    Measured: Sixteen week

  3. Muscle Strength

    Muscle strength will be assessed with the isokinetic dynamometer Biodex System-4 Pro (Biodex, Shirley, New York), which is a valid and reliable method. The strength of right/left knee flexor, and extensor muscles of the participants will be determined by mean peak torque at '60°/sec and 180°/sec angular velocities.

    Measured: Sixteen week

  4. Flexibility

    Flexibility will be assessed with the sit-and-reach test, which is a valid, and reliable method. Participants will be asked to reach forward as far as possible three times without bending their knees after one trial. The obtained values (cm) will be recorded and the best value will be used for analysis.

    Measured: Sixteen week

Secondary outcomes (5)
  1. Forced Expiratory Volume in 1 Second (FEV1) (L/sec)

    Forced Expiratory Volume in 1 Second (FEV1) (L/sec) will be assessed with a spirometer (Minispir, Italy) device. Measurement will be taken with the participant seated and in the resting state. Primarily the nose latch will be fitted to prevent air leakage. Then, the participant will be asked to inhale as much as possible and then exhale as quickly and completely as possible. This process will be repeated 3 times, and the highest values will be used for analysis.

    Measured: Sixteen week

  2. Forced Vital Capasity (FVC) (L)

    Forced Vital Capasity (FVC) (L) will be assessed with a spirometer (Minispir, Italy) device. Measurement will be taken with the participant seated and in the resting state. Primarily the nose latch will be fitted to prevent air leakage. Then, the participant will be asked to inhale as much as possible and then exhale as quickly and completely as possible. This process will be repeated 3 times, and the highest values will be used for analysis.

    Measured: Sixteen week

  3. FEV1/FVC (%)

    FEV1/FVC (%) will be assessed with a spirometer (Minispir, Italy) device. Measurement will be taken with the participant seated and in the resting state. Primarily the nose latch will be fitted to prevent air leakage. Then, the participant will be asked to inhale as much as possible and then exhale as quickly and completely as possible. This process will be repeated 3 times, and the highest values will be used for analysis.

    Measured: Sixteen week

  4. Peak Expiratory Flow (PEF) (L/min)

    Peak Expiratory Flow (PEF) (L/min) will be assessed with a spirometer (Minispir, Italy) device. Measurement will be taken with the participant seated and in the resting state. Primarily the nose latch will be fitted to prevent air leakage. Then, the participant will be asked to inhale as much as possible and then exhale as quickly and completely as possible. This process will be repeated 3 times, and the highest values will be used for analysis.

    Measured: Sixteen week

  5. Life Quality

    Quality of life will be assessed with the Short Form-36 (SF-36), a valid and reliable scale developed by Ware et al. It includes mainly the physical and the mental function scores. The best score is "100" and the worst score is "0". Higher scores indicate better physical or mental functioning. The obtained physical and the mental function scores will be used for analysis.

    Measured: sixteen week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Mar 2023
  2. Study start15 Mar 2023
  3. Primary completion15 Jul 2023
  4. Study completion15 Jul 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Model description
A prospective clinic study with single group
Masking
None (open label)
Enrolment
29 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05777265
Sponsor's protocol ID
CBU-FTR-ES-O2
Status last verified
Aug 2023
First submitted
8 Mar 2023
Last updated
4 Aug 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The investigators do not want to share individual participant data

Questions about this trial

What is this clinical trial studying?

A study testing Circuit Training in people with Healthy Women, run by Manisa Celal Bayar University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Aug 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Body Mass Index (kg/m2) (time frame: Sixteen week). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Aug 2023.

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