Body Fat and Frequency of Resistance Training
21 декабря 2017 г. обновлено: Crisieli Maria Tomeleri, Universidade Estadual de Londrina
Effects of Different Frequency Low-volume Resistance Training on Body Fat in Obese Older: A Randomized Controlled Trial
This study compared different frequency low-volume resistance training (RT) on total, android, gynoid and trunk body fat in obese older women
Обзор исследования
Статус
Завершенный
Условия
Вмешательство/лечение
Подробное описание
The aim of this study was to compare the effect of resistance training with different frequencies on total, android, gynoid and trunk body fat in obese older women.
Recruitment was carried out through newspaper and radio advertisements, and home delivery flyers in residential neighborhoods.
All participants completed health history and physical activity questionnaires, and met the following inclusion criteria: 60 years of age or older, relative body fat ≥ 32 assessed by whole body dual-energy X-ray absorptiometry (DXA), physically independent, free from cardiac or orthopedic dysfunction that would have precluded them from performing the tests or the training program associated with the study, not receiving hormonal replacement therapy, and not performing physical exercise more than once a week in the six months preceding the beginning of the investigation.Written informed consent was obtained from all participants after a detailed description of study procedures was provided.
This study was conducted in accordance with the Declaration of Helsinki and approved by the local Ethics Research Committee, and was carried out over a period of 16 weeks, with 12 weeks dedicated to the resistance training program, and 4 weeks directed to testing.
Anthropometric, body composition, and dietary intake measurements were performed during weeks 1-2, and 15-16.
A supervised progressive resistance training was performed between weeks 3-14.
The control group did not perform any type of organized physical exercise during the study period.
Supervised resistance training was performed during the 12 weeks of training.
All participants were individually supervised by physical education professionals throughout each training session to ensure that the study's training protocol was followed and to ensure subject safety.
The group 2X performed the program twice a week (Tuesdays and Thursdays), while group 3X performed three sessions a week (Mondays, Wednesdays, and Fridays).
The progression of training loads in each exercise occurred, when a participant completed 15 repetitions in two consecutive sessions, with increases of 2-5% in exercises for the upper limbs, and 5-10% in exercises for the lower limbs.
At the end of each session, one static stretching exercise at the point of discomfort for 15 seconds was performed for all major muscle groups for a total of exercises.
Participants were asked not to perform any other type of organized physical exercise during the entire study period.
Тип исследования
Интервенционный
Регистрация (Действительный)
63
Фаза
- Непригодный
Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
60 лет и старше (Взрослый, Пожилой взрослый)
Принимает здоровых добровольцев
Да
Полы, имеющие право на обучение
Женский
Описание
Inclusion Criteria:
- 60 years of age or older;
- relative body fat ≥ 32 assessed by whole body dual-energy X-ray absorptiometry (DXA);
- physically independent;
- free from cardiac or orthopedic dysfunction that would have precluded them from performing the tests or the training program associated with the study;
- not receiving hormonal replacement therapy;
- not performing physical exercise more than once a week in the six months preceding the beginning of the investigation.
Exclusion Criteria:
• All subjects not participating in 85% of the total sessions of training or withdrawl
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Факторное присвоение
- Маскировка: Одинокий
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Активный компаратор: Intervention 2X/week (G2X)
This group performed resistance training twice a week (Tuesdays and Thursdays)
|
Participants performed resistance training (RT) composed of eight exercises performed for one set of 10-15 repetition maximum (RM).
The rest interval between exercises was 2-3 min.
Participants were instructed to control the speed of movement in the ratio of 1:2 for concentric and eccentric muscle actions, respectively.
The progression of training loads in each exercise occurred, when a participant completed 15 repetitions in two consecutive sessions, with increases of 2-5% in exercises for the upper limbs, and 5-10% in exercises for the lower limbs.
At the end of each session, one static stretching exercise at the point of discomfort for 15 seconds was performed for all major muscle groups for a total of exercises.
Participants were asked not to perform any other type of organized physical exercise during the entire study period.
|
|
Активный компаратор: Intervention 3X/week (G3X)
This group performed resistance training three sessions a week (Mondays, Wednesdays, and Fridays).
|
Participants performed resistance training (RT) composed of eight exercises performed for one set of 10-15 repetition maximum (RM).
The rest interval between exercises was 2-3 min.
Participants were instructed to control the speed of movement in the ratio of 1:2 for concentric and eccentric muscle actions, respectively.
The progression of training loads in each exercise occurred, when a participant completed 15 repetitions in two consecutive sessions, with increases of 2-5% in exercises for the upper limbs, and 5-10% in exercises for the lower limbs.
At the end of each session, one static stretching exercise at the point of discomfort for 15 seconds was performed for all major muscle groups for a total of exercises.
Participants were asked not to perform any other type of organized physical exercise during the entire study period.
|
|
Без вмешательства: Control group (GC)
This group did not perform any type of organized physical exercise during the study period.
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Change in body composition
Временное ограничение: baseline and 12 weeks
|
Whole-body dual-energy X-ray absorptiometry (DXA) scans (Lunar Prodigy, model NRL 41990, GE Lunar, Madison, WI) were used to assess total body fat, trunk fat, gynoid fat and android fat.
Prior to scanning, participants were instructed to remove all objects containing metal.
Scans were performed with the subjects lying in the supine position along the table's longitudinal centerline axis.
Feet were taped together at the toes to immobilize the legs while the hands were maintained in a pronated position within the scanning region.
Both calibration and analysis were carried out by a skilled laboratory technician.
Equipment calibration followed the manufacturer's recommendations.
The software generated standard lines that set apart the limbs from the trunk and head.
These lines were adjusted by the same technician using specific anatomical points determined by the manufacturer.
The results are presented in kilograms (kg)
|
baseline and 12 weeks
|
|
Change in fat z-score
Временное ограничение: baseline and 12 weeks
|
A composite z-score, was calculated using the following formula: (total body fat z-score) + (gynoid body fat z-score) + (android fat z-score) / 3. Z-scores were obtained from the DXA using standard software.
|
baseline and 12 weeks
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Changes in Anthropometry Parameters
Временное ограничение: baseline and 12 weeks
|
Body mass was measured to the nearest 0.1 kg using a calibrated electronic scale (Balmak, Laboratory Equipment Labstore, Curitiba, Paraná, Brazil), with the participants wearing light workout clothing and no shoes.
Height was measured with a stadiometer attached to the scale to the nearest 0.1 cm, with subjects standing without shoes.
These parameter will be combined to report body mass index that will be calculate as body mass in kilograms divided by the square of height in meters.
|
baseline and 12 weeks
|
|
Changes in Dietary intake
Временное ограничение: baseline and 12 weeks
|
Participants were instructed by a dietitian to complete a food record on three nonconsecutive days (two week days and one weekend day) pre- and post-intervention.
Participants were given specific instructions regarding the recording of portion sizes and quantities to identify all food and fluid intake, in addition to viewing food models in order to enhance precision.
The amount of protein, carbohydrate, and lipid were calculated using nutrition analysis software (Avanutri Processor Nutrition Software, Rio de Janeiro, Brazil; Version 3.1.4).
The sum of the three macronutrients will be presented by total energy intake which will be expressed per kcal/kg per day.
|
baseline and 12 weeks
|
|
Changes in Total Strength
Временное ограничение: baseline and 12 weeks
|
Maximal dynamic strength was evaluated using the one repetition maximum (1RM) test assessed in the chest press, knee extension, and preacher curl exercises, performed in this exact order.
Testing for each exercise was preceded by a warmup set (6-10 repetitions), with approximately 50% of the estimated load used in the first attempt of the 1RM.
This warmup was also used to familiarize the subjects with the testing equipment and lifting technique.
The testing procedure was initiated 2 minutes after the warm-up.
The subjects were instructed to try to accomplish two repetitions with the imposed load and were given three attempts in both exercises.
The rest period was 3 to 5 min between each attempt, and 5 min between exercises.
The 1RM was recorded as the final load lifted in which the subject was able to complete only one single maximal execution.
Total strength was determined by the sum of the 3 exercises, expressed in kg.
|
baseline and 12 weeks
|
Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования (Действительный)
2 марта 2015 г.
Первичное завершение (Действительный)
6 июля 2015 г.
Завершение исследования (Действительный)
24 июля 2015 г.
Даты регистрации исследования
Первый отправленный
18 декабря 2017 г.
Впервые представлено, что соответствует критериям контроля качества
21 декабря 2017 г.
Первый опубликованный (Действительный)
22 декабря 2017 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
22 декабря 2017 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
21 декабря 2017 г.
Последняя проверка
1 декабря 2017 г.
Дополнительная информация
Термины, связанные с этим исследованием
Другие идентификационные номера исследования
- UEL09167-2/2015
Планирование данных отдельных участников (IPD)
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НЕТ
Информация о лекарствах и устройствах, исследовательские документы
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Нет
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Нет
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .