Obesity & OverweightRCTNCT07705750
Effects of Adapted Taekwondo Versus Conventional Training on Anthropometric Variables and Physical Function in Older Women With Abdominal Obesity
A study testing taekwondo training, multicomponent training and walking exercise in people with Obesity & Overweight and Older Women, run by Universidad Católica del Maule.
Trial summary
Therefore, this study aimed to analyze the effects of TKD on anthropometric and physical function parameters in older women with abdominal obesity, compared with conventional exercise interventions such as MCT, and WE. Read more about this study
- Who is it for?
- Ages 60 to 65 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Obesity & Overweight, Older Women
- What is being tested?
- taekwondo training, multicomponent training and walking exercise
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 70 participants
- Where
- No sites listed yet
- Study dates
- 7 Jul 2026to 13 Dec 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 60 to 65 years
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- (i) women aged 60-65 years
- (ii) waist circumference >88 cm
- (iii) ability to understand and follow contextualized instructions based on simple commands
- (iv) functional independence, defined as a score of ≥43 points on the Preventive Medicine Examination for Older Adults of the Chilean Ministry of Health.
- (v) capacity to comply with at least 85% of the scheduled intervention sessions.
Who cannot join
- (i) presence of disability
- (ii) participation in physical rehabilitation or presence of musculoskeletal injuries limiting usual physical activity
- (iii) permanent or temporary contraindication to participation in physical exercise.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Effects of Adapted Taekwondo Versus Conventional Training on Anthropometric Variables and Physical Function in Older Women With Abdominal Obesity: a Randomized Controlled Trial.
Therefore, this study aimed to analyze the effects of TKD on anthropometric and physical function parameters in older women with abdominal obesity, compared with conventional exercise interventions such as MCT, and WE. We hypothesized that TKD would produce greater improvements in abdominal fat and physical function than MCT and WE in older women with abdominal obesity.
Read the detailed description
This study was designed as a randomized, repeated-measures, double-blind controlled trial with a quantitative approach and three parallel intervention arms: taekwondo training (TKD), multicomponent training (MCT), and walking exercise (WE). The intervention period lasted 16 weeks, comprising 48 sessions delivered three times per week on Mondays, Wednesdays, and Fridays, with each session lasting 60 min. The outcomes assessed included anthropometric indicators, such as BMI, waist circumference, waist-to-height ratio, body fat percentage, and fat-free mass, as well as physical function, maximal isometric handgrip strength, and postural balance. All evaluations were conducted in the morning, between 10:00 and 12:00, at the same facilities, including the sports center and community headquarters. Environmental conditions, such as temperature, were controlled, and the same evaluators performed the baseline and post-intervention assessments. No musculoskeletal or cardiorespiratory injuries were reported during the intervention period, and participants did not report pain either before the assessments or during the training sessions.
- Conditions
- Obesity & Overweight, Older Women
- Being tested
- taekwondo training, multicomponent training, walking exercise
- Keywords
- combat sport
- Medical subject headings
- Obesity, Overweight
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
taekwondo trainingBehavioural
Also called TKD
The TKD program consisted of non-contact exercises performed during the main section of each session. This component included 10 min of basic stances and upper-limb technical actions, such as blocks and strikes, followed by 20 min of lower-limb techniques, including movements, stances, and kicks. These exercises were performed individually and in pairs, with and without taekwondo pads and shields. In addition, specific choreographies or poomsae, including Kibom Poomsae and Il Jang, were practiced for 10 min. During the first four weeks, participants completed three sets of eight repetitions of specific upper- and lower-limb technical exercises, with 2 min of rest between sets From weeks 5 to 8, training volume increased to four sets of eight repetitions for each technical exercise, maintaining 2 min of recovery between sets.
multicomponent trainingBehavioural
Also called MCT
program was organized as a 40-min circuit using elastic bands, poles, 2-kg medicine balls, and chairs. The main section included exercises aimed at improving agility, postural balance, and cardiorespiratory fitness. Strength exercises involved major lower-limb muscle groups, including the quadriceps, hamstrings, gluteal muscles, and gastrocnemius, as well as upper-limb and trunk-related muscles such as the biceps, triceps, deltoids, and latissimus dorsi. During the first four weeks, the training volume consisted of three sets of 10 repetitions for each strength exercise, with 2 min of rest between sets. Movement execution was controlled, with approximately 2 s for the concentric phase and 4 s for the eccentric phase. From weeks 5 to 8, the volume increased to four sets of 10 repetitions per exercise, maintaining 2 min of rest between sets. During weeks 9 to 12, four sets were maintained, while repetitions increased to 12. In the final phase, from weeks 13 to 16.
walking exerciseBehavioural
program began with a 5-min warm-up that included joint mobility and flexibility exercises. The main section consisted of walking on level ground for 35 to 50 min, with duration progressively increased by 5 min every four weeks. Each session ended with a 5-min cool-down involving static and dynamic flexibility exercises. Exercise intensity was maintained at a moderate-to-vigorous level, corresponding to 50% to 70% of HRmax, and was monitored using heart rate sensor straps (H10, Polar Electro Oy, Kempele, Finland). Training progression was adjusted every four weeks by increasing walking duration by 5 min and individually regulating cadence, thereby increasing the distance covered by each participant. Perceived exertion was also assessed using Borg's 10-point scale. and complemented with heart rate monitoring. Figure 2 summarizes the evaluation schedule and intervention sessions.
| Study group | Role | What they receive |
|---|---|---|
| walking exercise | Active comparator | The WE program began with a 5-min warm-up that included joint mobility and flexibility exercises. Receives: Behavioral: walking exercise |
| multicomponent training | Experimental | The MCT program was organized as a 40-min circuit using elastic bands, poles, 2-kg medicine balls, and chairs. Receives: Behavioral: multicomponent training |
| taekwondo training | Experimental | The TKD program consisted of non-contact exercises performed during the main section of each session. This component included 10 min of basic stances and upper-limb technical actions, such as blocks and strikes, followed by 20 min of lower-limb techniques, including movements, stances, and kicks. Receives: Behavioral: taekwondo training |
What is being measured
The primary outcome is the main question the study is designed to answer.
Body mass
Body mass was assessed using a digital scale (Seca 769, Germany; precision 0.1 kg), while standing height was measured with a stadiometer (Seca 220, Germany; precision 0.1 cm).
Measured: 16 weeks
Body mass index (BMI)
was calculated as body mass in kilograms divided by height in meters squared.
Measured: 16 weeks
Abdominal obesity
Abdominal obesity was classified according to waist circumference, using a cut-off point of ≥88 cm for women.
Measured: 16 weeks
Senior Fitness Test battery
Lower-limb muscle strength was determined through the 30-s chair stand test, recording the total number of repetitions completed within 30 s. Upper-limb muscle strength was assessed with the arm curl test, in which participants performed as many repetitions as possible in 30 s using a 3-pound dumbbell. Cardiorespiratory fitness was measured using the 2-min step test, which records the number of knee raises performed to the required height, corresponding approximately to 70° of hip flexion. Lower-body flexibility was assessed with the chair sit-and-reach test and expressed in centimeters. Upper-body flexibility was evaluated using the back scratch test, also reported in centimeters. Agility and dynamic balance were assessed using the timed up-and-go test, in which participants walked around a cone placed 8 feet (2.44 m) away, with performance recorded in seconds.
Measured: 16 weeks
Maximal Isometric Handgrip Strength
Maximal isometric handgrip strength was measured using a hydraulic hand dynamometer (Camry, model EH101, Zhongshan, China), following previously described procedures. Participants were seated with the shoulder slightly abducted, the elbow flexed, the forearm in a neutral position, and the wrist maintained in neutral alignment. The dynamometer was adjusted according to each participant's hand size to ensure a comfortable and functional grip, allowing adequate flexion of the metacarpophalangeal and interphalangeal joints and appropriate contact between the thumb and index finger. Each participant performed three trials with each hand, separated by 120 s of rest, and the highest value obtained across the attempts was used for analysis.
Measured: 16 weeks
Postural Balance
Postural balance was assessed by measuring center-of-pressure displacement using a force platform (ArtOficio Ltd., Valparaíso, Chile), according to previously reported recommendations. Data were collected at a sampling frequency of 40 Hz. Balance was evaluated under two visual conditions: eyes open and eyes closed, with each trial lasting 30 s. Participants were instructed to stand barefoot in a bipedal position, with their feet approximately shoulder-width apart, arms relaxed alongside the body, and to remain as still as possible throughout the assessment. Center-of-pressure area and velocity were calculated using Matlab R2012a software (MathWorks Inc., Natick, MA, USA).
Measured: 16 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Jul 2026
- Study start7 Jul 2026 (estimated)
- Primary completion20 Aug 2026 (estimated)
- Study completion13 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obesity & OverweightStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This study was designed as a randomized, repeated-measures, double-blind controlled trial with a quantitative approach and three parallel intervention arms: taekwondo training (TKD), multicomponent training (MCT), and walking exercise (WE).
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 70 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universidad Católica del Maule
- Sponsor type
- University, hospital or other
- Collaborators
- University of Talca
- Responsible party
- Principal investigator, Pablo Valdés-Badilla, Universidad Católica del Maule
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07705750
- Sponsor's protocol ID
- (n. 29-2022)
- Other IDs
- 29
- Acronym
- RCT
- Status last verified
- Jul 2026
- First submitted
- 7 Jul 2026
- Last updated
- 15 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Confidentiality of the data will be generated, as expressed in the ethics committee
Study at a glance
From the registry record, last updated by the sponsor on 15 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Adapted Taekwondo Versus Conventional Training on Anthropometric Variables and Physical Function in Older Women With Abdominal Obesity: a Randomized Controlled Trial.
- ClinicalTrials.gov ID
- NCT07705750
- Acronym / sponsor ID
- RCT / (n. 29-2022)
- Conditions
- Obesity & Overweight, Older Women
- Keywords
- combat sport
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 70 participants (estimated)
- Lead sponsor
- Universidad Católica del MauleUniversity, hospital or other
- Collaborators
- University of Talca
- Study start
- 7 Jul 2026 (estimated)
- Primary completion
- 20 Aug 2026 (estimated)
- Study completion
- 13 Dec 2026 (estimated)
- First posted
- 15 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Therefore, this study aimed to analyze the effects of TKD on anthropometric and physical function parameters in older women with abdominal obesity, compared with conventional exercise interventions such as MCT, and WE. We hypothesized that TKD would produce greater improvements in abdominal fat and physical function than MCT and WE in older women with abdominal obesity.
Detailed description
This study was designed as a randomized, repeated-measures, double-blind controlled trial with a quantitative approach and three parallel intervention arms: taekwondo training (TKD), multicomponent training (MCT), and walking exercise (WE). The intervention period lasted 16 weeks, comprising 48 sessions delivered three times per week on Mondays, Wednesdays, and Fridays, with each session lasting 60 min. The outcomes assessed included anthropometric indicators, such as BMI, waist circumference, waist-to-height ratio, body fat percentage, and fat-free mass, as well as physical function, maximal isometric handgrip strength, and postural balance. All evaluations were conducted in the morning, between 10:00 and 12:00, at the same facilities, including the sports center and community headquarters. Environmental conditions, such as temperature, were controlled, and the same evaluators performed the baseline and post-intervention assessments. No musculoskeletal or cardiorespiratory injuries were reported during the intervention period, and participants did not report pain either before the assessments or during the training sessions.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 3
- Model description
- This study was designed as a randomized, repeated-measures, double-blind controlled trial with a quantitative approach and three parallel intervention arms: taekwondo training (TKD), multicomponent training (MCT), and walking exercise (WE).
| Arm | Type | Receives |
|---|---|---|
| walking exercise | Active comparator | Behavioral: walking exerciseThe WE program began with a 5-min warm-up that included joint mobility and flexibility exercises. |
| multicomponent training | Experimental | Behavioral: multicomponent trainingThe MCT program was organized as a 40-min circuit using elastic bands, poles, 2-kg medicine balls, and chairs. |
| taekwondo training | Experimental | Behavioral: taekwondo trainingThe TKD program consisted of non-contact exercises performed during the main section of each session. This component included 10 min of basic stances and upper-limb technical actions, such as blocks and strikes, followed by 20 min of lower-limb techniques, including movements, stances, and kicks. |
Who may qualify
- Ages
- 60 to 65 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- (i) women aged 60-65 years
- (ii) waist circumference >88 cm
- (iii) ability to understand and follow contextualized instructions based on simple commands
- (iv) functional independence, defined as a score of ≥43 points on the Preventive Medicine Examination for Older Adults of the Chilean Ministry of Health.
- (v) capacity to comply with at least 85% of the scheduled intervention sessions.
Key exclusion criteria (3 listed)
- (i) presence of disability
- (ii) participation in physical rehabilitation or presence of musculoskeletal injuries limiting usual physical activity
- (iii) permanent or temporary contraindication to participation in physical exercise.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| taekwondo trainingAlso: TKDThe TKD program consisted of non-contact exercises performed during the main section of each session. This component included 10 min of basic stances and upper-limb technical actions, such as blocks and strikes, followed by 20 min of lower-limb techniques, including movements, stances, and kicks. These exercises were performed individually and in pairs, with and without taekwondo pads and shields. In addition, specific choreographies or poomsae, including Kibom Poomsae and Il Jang, were practiced for 10 min. During the first four weeks, participants completed three sets of eight repetitions of specific upper- and lower-limb technical exercises, with 2 min of rest between sets From weeks 5 to 8, training volume increased to four sets of eight repetitions for each technical exercise, maintaining 2 min of recovery between sets. | Behavioural | taekwondo training |
| multicomponent trainingAlso: MCTprogram was organized as a 40-min circuit using elastic bands, poles, 2-kg medicine balls, and chairs. The main section included exercises aimed at improving agility, postural balance, and cardiorespiratory fitness. Strength exercises involved major lower-limb muscle groups, including the quadriceps, hamstrings, gluteal muscles, and gastrocnemius, as well as upper-limb and trunk-related muscles such as the biceps, triceps, deltoids, and latissimus dorsi. During the first four weeks, the training volume consisted of three sets of 10 repetitions for each strength exercise, with 2 min of rest between sets. Movement execution was controlled, with approximately 2 s for the concentric phase and 4 s for the eccentric phase. From weeks 5 to 8, the volume increased to four sets of 10 repetitions per exercise, maintaining 2 min of rest between sets. During weeks 9 to 12, four sets were maintained, while repetitions increased to 12. In the final phase, from weeks 13 to 16. | Behavioural | multicomponent training |
| walking exerciseprogram began with a 5-min warm-up that included joint mobility and flexibility exercises. The main section consisted of walking on level ground for 35 to 50 min, with duration progressively increased by 5 min every four weeks. Each session ended with a 5-min cool-down involving static and dynamic flexibility exercises. Exercise intensity was maintained at a moderate-to-vigorous level, corresponding to 50% to 70% of HRmax, and was monitored using heart rate sensor straps (H10, Polar Electro Oy, Kempele, Finland). Training progression was adjusted every four weeks by increasing walking duration by 5 min and individually regulating cadence, thereby increasing the distance covered by each participant. Perceived exertion was also assessed using Borg's 10-point scale. and complemented with heart rate monitoring. Figure 2 summarizes the evaluation schedule and intervention sessions. | Behavioural | walking exercise |
Primary outcome
Body mass
Time frame: 16 weeks
Body mass was assessed using a digital scale (Seca 769, Germany; precision 0.1 kg), while standing height was measured with a stadiometer (Seca 220, Germany; precision 0.1 cm).
Body mass index (BMI)
Time frame: 16 weeks
was calculated as body mass in kilograms divided by height in meters squared.
Abdominal obesity
Time frame: 16 weeks
Abdominal obesity was classified according to waist circumference, using a cut-off point of ≥88 cm for women.
Senior Fitness Test battery
Time frame: 16 weeks
Lower-limb muscle strength was determined through the 30-s chair stand test, recording the total number of repetitions completed within 30 s. Upper-limb muscle strength was assessed with the arm curl test, in which participants performed as many repetitions as possible in 30 s using a 3-pound dumbbell. Cardiorespiratory fitness was measured using the 2-min step test, which records the number of knee raises performed to the required height, corresponding approximately to 70° of hip flexion. Lower-body flexibility was assessed with the chair sit-and-reach test and expressed in centimeters. Upper-body flexibility was evaluated using the back scratch test, also reported in centimeters. Agility and dynamic balance were assessed using the timed up-and-go test, in which participants walked around a cone placed 8 feet (2.44 m) away, with performance recorded in seconds.
Maximal Isometric Handgrip Strength
Time frame: 16 weeks
Maximal isometric handgrip strength was measured using a hydraulic hand dynamometer (Camry, model EH101, Zhongshan, China), following previously described procedures. Participants were seated with the shoulder slightly abducted, the elbow flexed, the forearm in a neutral position, and the wrist maintained in neutral alignment. The dynamometer was adjusted according to each participant's hand size to ensure a comfortable and functional grip, allowing adequate flexion of the metacarpophalangeal and interphalangeal joints and appropriate contact between the thumb and index finger. Each participant performed three trials with each hand, separated by 120 s of rest, and the highest value obtained across the attempts was used for analysis.
Postural Balance
Time frame: 16 weeks
Postural balance was assessed by measuring center-of-pressure displacement using a force platform (ArtOficio Ltd., Valparaíso, Chile), according to previously reported recommendations. Data were collected at a sampling frequency of 40 Hz. Balance was evaluated under two visual conditions: eyes open and eyes closed, with each trial lasting 30 s. Participants were instructed to stand barefoot in a bipedal position, with their feet approximately shoulder-width apart, arms relaxed alongside the body, and to remain as still as possible throughout the assessment. Center-of-pressure area and velocity were calculated using Matlab R2012a software (MathWorks Inc., Natick, MA, USA).
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Jul 2026.
- Individual participant dataSharing planned: No. Confidentiality of the data will be generated, as expressed in the ethics committee
Related trials for Obesity & Overweight
RecruitingObservational study
Endoscopic Sleeve Gastroplasty (ESG) Prospective Trial for Obesity (EGO-Trial)
Obesity
Active, not recruitingPhase 4
Effects of Sequential Therapy With Mexidol® (Intravenous) and Mexidol® FORTE 250 (Oral) on Functional Brain Activity Assessed by Functional Magnetic Resonance Imaging and Biochemical Parameters in Patients With Chronic Cerebral Ischemia: A Comparison of Patients With and Without Metabolic Disorders
Metabolic Abnormalities, Obesity & Overweight
Recruiting
Exercise Training and Vitamin D Metabolism
Obesity & Overweight, Vitamin D
Recruiting
Metabolic Health, Bones and Nuts During Weight Loss in Adults
Weight Loss, Bone Density
Active, not recruiting
Effect of Probiotics on Insulin Sensitivity in Overweight and Obese Pregnancy
Obesity & Overweight, Gestational Diabetes Mellitus (GDM)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
A study testing taekwondo training, multicomponent training and walking exercise in people with Obesity & Overweight and Older Women, run by Universidad Católica del Maule.
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 5 inclusion and 3 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: opening soon, as of the sponsor's last update on 15 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Pablo Váldes, PhD (+56953646566, valdesbadilla@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Body mass (time frame: 16 weeks). The study lists 6 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 15 Jul 2026; AzTrials last refreshed its copy on 7 Nov 2026.