Insulin Growth Factor I DeficiencyNCT05642169
Effect of a HIIT Program on Quality of Life, Executive Functions, and IGF-1 Response in Sedentary Young University Women
A study testing HIIT, HIIT+PA and CON in people with Insulin Growth Factor I Deficiency and IGF1 Deficiency, run by University of Seville at 1 site in Spain.
Trial summary
Sedentary lifestyle, understood as an activity that requires minimal body movement (Tremblay et al., 2017), is one of the main factors responsible for chronic diseases in Young adults. Read more about this study
- Who is it for?
- Ages 18 to 30 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Insulin Growth Factor I Deficiency, IGF1 Deficiency, Executive Function Disorder
- What is being tested?
- HIIT, HIIT+PA and CON
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 75 participants
- Where
- 1 siteSpain
- Study dates
- 15 Oct 2022to 15 Apr 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 30 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Age: 18-30 years old
- Reflect in the IPAQ questionnaire to be in category 1 or low level of physical activity (Craig et al., 2003) and therefore not conform to the minimum recommendations for physical activity and physical exercise proposed by the WHO.
- Not suffering from somatic signs or serious psychiatric illnesses that prevent the practice of physical exercise.
- Not attending psychological therapies in the last 12 months prior to the study. The use of this type of treatment may have an impact on the improvement of cognitive abilities and executive functions of the study population.
- Being able to communicate.
- Informed consent: Be able and willing to give informed consent.
Who cannot join
- Having a general cognitive impairment or executive function disorder recognized and treated by specialists.
- Physical activity: In order to select sedentary subjects, we excluded those who engaged in physical activity in their leisure time in a continuous and planned manner.
- Bilingualism: Habitual and indistinct use of two or more languages. This may condition the results in various cognitive tests present in the study, since it is known that this intellectual capacity has a morphological and functional impact on the brain.
- Musical instrument: Playing a musical instrument regularly and continuously, as in the previous criterion, generates a positive effect on the subject's cognition
Trial locations and contacts
1 site in 1 country.
Spain1 site, 1 recruiting
- Recruiting
Education Faculty
Seville, 41013
manuel jesus j roldan, 650344644, manueljr@euosuna.org
jimenez.roldan.manueljesus@gmail.com
About this study
Official title: Effect of a High Interval Intensity Training Program on Quality of Life, Mental Health, Brain Executive Functions, and IGF-1 Response in Sedentary Young University Women.
Sedentary lifestyle, understood as an activity that requires minimal body movement (Tremblay et al., 2017), is one of the main factors responsible for chronic diseases in Young adults.
In addition, this sedentary lifestyle generates mental disorders, such as anxiety, low self-esteem and depression, being more pronounced in women than in men (Nihill et al., 2013). Thus, both daily physical activity (PA) and physical exercise programs (PE), of moderate-vigorous intensity, act as an effective tools for the improvement of quality of life, since they generate benefits at physiological, psychological and social levels (Cohen et al., 2019).
Read more
If we focus on young adult, it can be seen how there is a significant decrease in the practice of physical exercise at this age (Grim et al., 2011). This means that the aforementioned recommendations are not reached (Cancela et al., 2019). Furthermore, if compared between sexes, lower levels are shown in the female sex (King et al., 2014).
For this reasons, and taking into account that the female population is a population vulnerable to significantly reduce their physical activity practice with age (Cohen et al., 2019), it is interesting to investigate on the possible health-related factors that this entails, such as quality of life, physical condition and mental health.
For these reasons, it is necessary to create effective strategies to address factors related to the main cognitive impairments and thus preserve better mental health.
Among all possible strategies, both pharmacological and non-pharmacological for the improvement of mental health, cognition and executive functions in young adults.Physical exercise has been shown to be a highly effective strategy at these ages (Heath et al., 2016). The stimulation of HIIT seems to reduce antioxidant responses. In recent years, there is a high interest in knowing the effect of HIIT on different health outcomes, such as physical and psychological fitness (Eather et al., 2019).
For all these reasons, sedentary lifestyles are an important public health factor associated with numerous pathologies and have been shown to have a significant cognitive involvement. Although we know that physical exercise can have a preventive role in the management of these associations, the conditioning factors of physical exercise are unknown, as well as the lifestyle factors that could contribute to a greater extent to the improvement of executive functionality in young women.
Read the detailed description
The present investigation follows a randomized controlled experimental design (RCT), of sequential type, with parallel groups with three groups and repeated measures, being evaluated in a pretest, posttest and after the end of the follow-up period.
The sample, of casual or incidental type, was randomly distributed in two experimental groups and a control group, thus avoiding selection bias.
Once the study population had been selected and met the established inclusion and exclusion criteria, a 12-week HIIT-based intervention was performed.
Two of the experimental groups will perform this training program with the only difference that the HIIT+PA group will have to perform 10,000 steps per day, thus increasing daily physical activity.
Among the main study variables were insulin-like growth factor-1 (IGF-1), executive functions, physical condition, physical activity, quality of life and body composition.
- Being tested
- HIIT, HIIT+PA, CON
- Keywords
- HIIT, IGF-1, young adult, women
- Medical subject headings
- Insulin-Like Growth Factor I Deficiency
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HIITBehavioural
The training sessions will have a frequency of 3 times per week (Monday, Wednesday and Friday) and the duration will be between 39 to 54 minutes, depending on the training week.
The training program will be developed with the own body weight of each participant. Therefore, a progression according to the needs of this population will be fulfilled. The session model could be multi-joint exercises with self-loads, where the difficulty of the exercises will be worked progressively. Throughout the main part of each workout, 30 seconds of work will be performed at the corresponding intensity and 30 seconds of rest. Halfway through the total repetitions, there will be 2 minutes of recovery.
HIIT+PABehavioural
In relation to the 2 groups that will perform HIIT, the HIIT+AF will have to complete 10.000 steps per day. In this way, they will be focusing on increasing their daily physical activity. In addition, this group will perform the same HIIT training programme as the other experimental group.
CONBehavioural
This group will not suffer any changes in their lifestyle
| Study group | Role | What they receive |
|---|---|---|
| HIIT | Experimental | Training program for 12 weeks with a frequency of 3 workouts per week. Receives: Behavioral: HIIT |
| HIIT+AF | Experimental | They will develop the same training program as the HIIT group, and they will also have to perform 10,000 steps per day. Receives: Behavioral: HIIT+PA |
| Control | Placebo comparator | They will not suffer any change in their lifestyle. Receives: Behavioral: CON |
What is being measured
The primary outcome is the main question the study is designed to answer.
Biochemical determinants
The main biochemical determinants established in this study will be measured in saliva. Thus, the magnitude of the IGF-1 response in saliva as a consequence of the execution of a 12-week HIIT training program will be analyzed. In addition, the acute response to maximal effort will be measured at the initial and final assessments.
Saliva will be collected in a fasted state (between 8-12 hours) and the passive drooling method will be used. At each assessment, a saliva sample will be obtained at rest and after maximal effort.
To measure the variability in each assessment of IGF-1 concentration in saliva, the ELISA KIT protocol will be used.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Secondary outcomes (11)
Body composition
Body composition will be measured by taking waist and hip perimeters and through electrical bioimpedance (BIA). This is a fast and non-invasive technique in which different body composition variables are estimated. Such a tool becomes a reliable system with scientific validity (Kelly \& Metcalfe, 2012).
The BIA used in this investigation (Tanita BC-418, Tokyo, Japan) is a segmental measurement. The subject is placed in a standing position on 4 electrodes, located on the feet and hands, where through two of them an alternating current is introduced and the remaining two collect this current, measuring, among others, the values of impedance, resistance and body reactance.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Maximum oxygen consumption
Maximum oxygen consumption (VO2max) will be estimated from the maximum power output (MPO) achieved in an incremental cycloergometer test (Andersen, 1995). Therefore, only the MPO will be taken into account for its estimation, since it is a measure of the capacity of the cardiorespiratory system, which can predict 80% of the variation in VO2max.
The development of the test begins with a first part of 7 minutes at a submaximal load of 69W. At the end of this phase the heart rate was recorded with a pulsometer (H10 Polar Electro OY, Finalandia). The load will be increased by 35W every 2 minutes until the subject reached exhaustion.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Physical activity and sedentary behaviour
Physical activity will be evaluated objectively by accelerometry. The accelerometer is a device that allows objective quantification of the physical activity performed by a person. The study population was asked to wear a triaxial accelerometer (GTX3, Penascola, Florida, USA).
Participants were instructed to wear the accelerometer throughout the day (24h). The placement of the accelerometer during the recording days should be on the right side at hip height and in line with the anterior face of the ipsilateral lower extremity. To avoid damage to the device, it was removed in any aquatic situation. On this occasion, a record sheet was provided for its annotation.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
SF-36 quality of life.
To detect changes in health-related quality of life, the SF-36 questionnaire will be used. This questionnaire, in its Spanish versión (Vilagut et al., 2005), focuses on assessing general health status through a generic scale. This provides a profile of quality of life, both of a general population and of specific subgroups.
This questionnaire consists of a total of 36 questions covering 8 health concepts. In addition, there are two summary measures, which are physical health and mental health. Mental health is divided into the vitality scale (4 items), social functioning (2), emotional role (3) and mental health (5). On the other hand, physical health encompasses physical capacity (10 items), physical role (4), bodily pain (2) and general health (5). In addition, two global questions on the perception of their health are added.
The scores for each scale range from 0 to 100, with higher scores indicating a better quality of life
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Rosenberg self-esteem scale.
The Rosenberg self-esteem scale (1965) is the most widely used test for the evaluation of self-esteem in scientific research and clinical practice.
This test is a 10-item scale for analyzing global self-esteem (Vázquez Morejón et al., 2004). Each item is classified on a 4-point Likert scale, where 1 is equivalent to "strongly disagree" and 4 to "strongly agree". Of the 10 questions asked, five are formulated positively and five negatively (2,5,8,9,10). In addition, each question measures the degree of satisfaction of the person together with the person's self-assessment.
In relation to the results, the unifactorial nature proposed by Rosenberg has been questioned; however, other authors support a bifactorial structure of positive and negative self-esteem. According to the validation study of this work in Spanish (Atienza et al., 2000), when the sample is made up of women, the elaboration of a single factor of global self-esteem is suggested.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Hamilton Rating Scale for the Evaluation of Depression (HDRS).
The HDRS (Hamilton, 1960) is a scale for assessing depression. It is hetero-applicable and is designed with the aim of quantitatively assessing the degree of depression of the interviewed subject.
The original version consists of 21 questions, but on this occasion the reduced versión (Hamilton, 1967) published later will be used. This version consists of 17 questions, which is recommended for clinical use.
The short version of the HDRS has been validated in the Spanish version (Ramos-Brieva \& Cordero Villafáfila, 1986) showing high reliability and sensitivity to change in different populations (Ramos-Brieva \& Cordero-Villafafila, 1988).
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Executive functions
The measurements of the following cognitive tests will be performed with the collaboration of a psychologist specialized in the execution and description of the following executive tests:
For the evaluation of inhibitory control, the Stroop testT will be used (Golden, 1999). This is a neuropsychological test that measures the interference generated in the performance of a task. In this work, the Victoria version will be developed in a digitized form (Mueller et al., 2012).
For the evaluation of cognitive flexibility, wil be used the Wisconsin card test (WCST) (Cepeda et al., 2000). It can be performed traditionally or, as in this case, digitally. This test consists of a total of 64 cards. The cards present different combinations according to 4 geometric shapes, 4 colors and 4 quantities.
Digit Span Test (DST) analyzes the ability to store and retain information, whose mission is to measure working memory.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Lower body muscle strength
Leg extension muscle strength will be assessed on a calibrated isokinetic dynamometer (Biodex System 4, Biodex Medical System, Inc., Shirley, NY, USA). Therefore, the Biodex System 4 will be used to assess each subject's ability to generate maximal isometric power with the knee extensor musculature in a 60° flexion joint position from a seated position.
For measurement, the Biodex clinical data station will be used to analyze the Biodex torque and position signals and obtain the resulting measurements.
The performance protocol will consist of executing two maximal isometric efforts for 5 seconds. The subject, with arms crossed over the chest, will begin to perform the maximal force at the evaluator's "push" voice. Subsequently, the subject will rest 30 seconds to perform the second attempt.
Once both attempts have been completed, the best result of the peak torque variable (N-M) will be recorded for further analysis.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Upper extremity muscle strength.
Upper extremity muscle strength will be assessed through manual dynamometry testing with a digital dynamometer (TKK 5101 Grip-D; Takey, Tokyo, Japan) as described in other studies (Ruiz-Ruiz et al., 2002).
Subjects were to be placed in a bipedal position during the test with the arms in full extension and without touching any part of the body with the dynamometer, except for the hand. The positioning of the body should be at all times with the shoulder girdle parallel to the ground, without allowing flexion or lateral movement of the trunk during the application of force.
The participants will be instructed to squeeze the dynamometer grip as hard as possible and without being able to bend any of the joints involved. The duration of the effort will be 5 seconds, without being able to perform discontinuous activations, i.e., they must maintain the maximum isometric force possible during the 5 seconds.
Finally, the best result (Kg) of the two tests performed will be recorded.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Beck Depression Inventory (BDI-II)
The Beck-II (Beck \& Steer, 1993) is used to measure depressive symptomatology.
It is a self-administered instrument consisting of 21 items that assess cognitive, affective and neurovegetative factors. This questionnaire is usually the most widely used in clinical psychology to assess the degree of depression (Sanz et al., 2003).
This questionnaire has been validated in the Spanish version (Sanz et al., 2005) and has also shown high reliability in a university population (Sprinkle et al., 2002).
Each item has four responses, ordered from least to most severe (from 0 to 3 points), and the subject must choose the sentence that most closely matches his or her perception during the last week. The scores of this instrument range from 0-63, with the reference cut-off points being the following: 0-9 no depression; 10-15 mild depression; 16-19 moderate depression; 20-29 moderate-severe depression; 30-63 severe depression.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
International Physical Activity Questionnaire (IPAQ).
The IPAQ questionnaire is an instrument to determine approximately the level of physical activity practiced by the general population (Hagstro et al., 2006). This questionnaire is one of the most widely used for the detection of sedentary lifestyles, used to a greater extent in its short version, adapted and translated into Spanish. In addition, this questionnaire shows excellent reliability (Craig et al., 2003) and high validity for its application in university population (Cancela et al., 2019).
Therefore, for the calculation of the IPAQ data, an average of Mets will be adopted for each type of activity, resulting as follows: walking 3.3 Mets, moderate activities 4.0 Mets and intense activities 8.0 Mets.
Measured: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Dec 2022
- Study start15 Oct 2022
- Primary completion15 Jan 2023 (estimated)
- Study completion15 Apr 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Insulin Growth Factor I DeficiencyStudies 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
- The present research follows a randomized controlled experimental design (RCT), sequential type, with parallel groups with three groups and repeated measures, being evaluated in a pretest, posttest and after the end of the follow-up period. The sample, of casual or incidental type, were randomly distributed in two experimental groups and one CG, thus avoiding selection bias. The CG continued to maintain their lifestyle on a daily basis. On the other hand, we found two experimental groups, which performed a HIIT program with a frequency of 3 workouts per week. In one of them (HIIT+AF), the focus was on increasing their daily physical activity through the execution of 10,000 steps per day. The other experimental group (HIIT) followed the same HIIT program.
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 75 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Seville
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jimenez-Roldan Manuel Jesus, University of Seville
- Investigators
- Manuel Jesus Jimenez Roldan, Principal investigator, University of Seville
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05642169
- Sponsor's protocol ID
- Young Brain Proyect
- Status last verified
- Nov 2022
- First submitted
- 18 Nov 2022
- Last updated
- 8 Dec 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Zhang Y, Zhang B, Gan L, Ke L, Fu Y, Di Q, Ma X. Effects of Online Bodyweight High-Intensity Interval Training Intervention and Health Education on the Mental Health and Cognition of Sedentary Young Females. Int J Environ Res Public Health. 2021 Jan 3;18(1):302. doi: 10.3390/ijerph18010302.
PubMed 33401605
Study at a glance
From the registry record, last updated by the sponsor on 8 Dec 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of a High Interval Intensity Training Program on Quality of Life, Mental Health, Brain Executive Functions, and IGF-1 Response in Sedentary Young University Women.
- ClinicalTrials.gov ID
- NCT05642169
- Acronym / sponsor ID
- Young Brain Proyect
- Keywords
- HIIT, IGF-1, young adult, women
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 75 participants (estimated)
- Lead sponsor
- University of SevilleUniversity, hospital or other
- Study start
- 15 Oct 2022 (actual)
- Primary completion
- 15 Jan 2023 (estimated)
- Study completion
- 15 Apr 2023 (estimated)
- First posted
- 8 Dec 2022 (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.
Sedentary lifestyle, understood as an activity that requires minimal body movement (Tremblay et al., 2017), is one of the main factors responsible for chronic diseases in Young adults.
In addition, this sedentary lifestyle generates mental disorders, such as anxiety, low self-esteem and depression, being more pronounced in women than in men (Nihill et al., 2013). Thus, both daily physical activity (PA) and physical exercise programs (PE), of moderate-vigorous intensity, act as an effective tools for the improvement of quality of life, since they generate benefits at physiological, psychological and social levels (Cohen et al., 2019).
If we focus on young adult, it can be seen how there is a significant decrease in the practice of physical exercise at this age (Grim et al., 2011). This means that the aforementioned recommendations are not reached (Cancela et al., 2019). Furthermore, if compared between sexes, lower levels are shown in the female sex (King et al., 2014).
For this reasons, and taking into account that the female population is a population vulnerable to significantly reduce their physical activity practice with age (Cohen et al., 2019), it is interesting to investigate on the possible health-related factors that this entails, such as quality of life, physical condition and mental health.
For these reasons, it is necessary to create effective strategies to address factors related to the main cognitive impairments and thus preserve better mental health.
Among all possible strategies, both pharmacological and non-pharmacological for the improvement of mental health, cognition and executive functions in young adults.Physical exercise has been shown to be a highly effective strategy at these ages (Heath et al., 2016). The stimulation of HIIT seems to reduce antioxidant responses. In recent years, there is a high interest in knowing the effect of HIIT on different health outcomes, such as physical and psychological fitness (Eather et al., 2019).
For all these reasons, sedentary lifestyles are an important public health factor associated with numerous pathologies and have been shown to have a significant cognitive involvement. Although we know that physical exercise can have a preventive role in the management of these associations, the conditioning factors of physical exercise are unknown, as well as the lifestyle factors that could contribute to a greater extent to the improvement of executive functionality in young women.
Detailed description
The present investigation follows a randomized controlled experimental design (RCT), of sequential type, with parallel groups with three groups and repeated measures, being evaluated in a pretest, posttest and after the end of the follow-up period.
The sample, of casual or incidental type, was randomly distributed in two experimental groups and a control group, thus avoiding selection bias.
Once the study population had been selected and met the established inclusion and exclusion criteria, a 12-week HIIT-based intervention was performed.
Two of the experimental groups will perform this training program with the only difference that the HIIT+PA group will have to perform 10,000 steps per day, thus increasing daily physical activity.
Among the main study variables were insulin-like growth factor-1 (IGF-1), executive functions, physical condition, physical activity, quality of life and body composition.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 3
- Model description
- The present research follows a randomized controlled experimental design (RCT), sequential type, with parallel groups with three groups and repeated measures, being evaluated in a pretest, posttest and after the end of the follow-up period. The sample, of casual or incidental type, were randomly distributed in two experimental groups and one CG, thus avoiding selection bias. The CG continued to maintain their lifestyle on a daily basis. On the other hand, we found two experimental groups, which performed a HIIT program with a frequency of 3 workouts per week. In one of them (HIIT+AF), the focus was on increasing their daily physical activity through the execution of 10,000 steps per day. The other experimental group (HIIT) followed the same HIIT program.
| Arm | Type | Receives |
|---|---|---|
| HIIT | Experimental | Behavioral: HIITTraining program for 12 weeks with a frequency of 3 workouts per week. |
| HIIT+AF | Experimental | Behavioral: HIIT+PAThey will develop the same training program as the HIIT group, and they will also have to perform 10,000 steps per day. |
| Control | Placebo comparator | Behavioral: CONThey will not suffer any change in their lifestyle. |
Who may qualify
- Ages
- 18 to 30 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (6 listed)
- Age: 18-30 years old
- Reflect in the IPAQ questionnaire to be in category 1 or low level of physical activity (Craig et al., 2003) and therefore not conform to the minimum recommendations for physical activity and physical exercise proposed by the WHO.
- Not suffering from somatic signs or serious psychiatric illnesses that prevent the practice of physical exercise.
- Not attending psychological therapies in the last 12 months prior to the study. The use of this type of treatment may have an impact on the improvement of cognitive abilities and executive functions of the study population.
- Being able to communicate.
Key exclusion criteria (4 listed)
- Having a general cognitive impairment or executive function disorder recognized and treated by specialists.
- Physical activity: In order to select sedentary subjects, we excluded those who engaged in physical activity in their leisure time in a continuous and planned manner.
- Bilingualism: Habitual and indistinct use of two or more languages. This may condition the results in various cognitive tests present in the study, since it is known that this intellectual capacity has a morphological and functional impact on the brain.
- Musical instrument: Playing a musical instrument regularly and continuously, as in the previous criterion, generates a positive effect on the subject's cognition
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 |
|---|---|---|
| HIITThe training sessions will have a frequency of 3 times per week (Monday, Wednesday and Friday) and the duration will be between 39 to 54 minutes, depending on the training week. The training program will be developed with the own body weight of each participant. Therefore, a progression according to the needs of this population will be fulfilled. The session model could be multi-joint exercises with self-loads, where the difficulty of the exercises will be worked progressively. Throughout the main part of each workout, 30 seconds of work will be performed at the corresponding intensity and 30 seconds of rest. Halfway through the total repetitions, there will be 2 minutes of recovery. | Behavioural | HIIT |
| HIIT+PAIn relation to the 2 groups that will perform HIIT, the HIIT+AF will have to complete 10.000 steps per day. In this way, they will be focusing on increasing their daily physical activity. In addition, this group will perform the same HIIT training programme as the other experimental group. | Behavioural | HIIT+AF |
| CONThis group will not suffer any changes in their lifestyle | Behavioural | Control |
Primary outcome
Biochemical determinants
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
The main biochemical determinants established in this study will be measured in saliva. Thus, the magnitude of the IGF-1 response in saliva as a consequence of the execution of a 12-week HIIT training program will be analyzed. In addition, the acute response to maximal effort will be measured at the initial and final assessments. Saliva will be collected in a fasted state (between 8-12 hours) and the passive drooling method will be used. At each assessment, a saliva sample will be obtained at rest and after maximal effort. To measure the variability in each assessment of IGF-1 concentration in saliva, the ELISA KIT protocol will be used.
11 secondary outcomes
Body composition
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Maximum oxygen consumption
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Physical activity and sedentary behaviour
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
SF-36 quality of life.
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Rosenberg self-esteem scale.
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Hamilton Rating Scale for the Evaluation of Depression (HDRS).
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Executive functions
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Lower body muscle strength
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Upper extremity muscle strength.
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Beck Depression Inventory (BDI-II)
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
International Physical Activity Questionnaire (IPAQ).
Time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Dec 2022.
- Results publication: PubMed 33401605Zhang Y, Zhang B, Gan L, Ke L, Fu Y, Di Q, Ma X. Effects of Online Bodyweight High-Intensity Interval Training Intervention and Health Education on the Mental Health and Cognition of Sedentary Young Females. Int J Environ Res Public Health. 2021 Jan 3;18(1):302. doi: 10.3390/ijerph18010302.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: No
Related trials for Insulin Growth Factor I Deficiency
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. This study is not recruiting at the moment.
Manuel Jesus Jimenez Roldan principal investigator
University of Seville
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing HIIT, HIIT+PA and CON in people with Insulin Growth Factor I Deficiency and IGF1 Deficiency, run by University of Seville at 1 site in Spain.
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 6 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: status not confirmed, as of the sponsor's last update on 8 Dec 2022. 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 Spain. 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. Some participants in this study may receive a placebo. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Manuel Jesús Jiménez Roldán (650344644, manueljr@euosuna.org), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Biochemical determinants (time frame: Up to 12 weeks (post) and through study completion, an average of 24 weeks (Follow-Up).). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05642169, which also lists 1 linked publication.
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 8 Dec 2022.