Effect of Acupuncture on Vascular Biomarkers and Psychological Well-Being of Women Undergoing IVF (AcupunctIVF)
11 сентября 2020 г. обновлено: Texas Tech University Health Sciences Center
Effect of Acupuncture on Vascular Biomarkers and Psychological Well-Being of Women Undergoing In Vitro Fertilization (IVF)
Experimental Approach: (1) Participants: Women (ages 21 to 42) who seek IVF treatment at the Center for Fertility & Reproductive Surgery will be eligible for the study.
Seventy women will be recruited and randomly assigned to either the intervention (acupuncture plus standard care) or the comparison (standard care alone) group.
(2) Intervention: Participants in the intervention group will receive 3 acupuncture sessions during the project with the first treatment between day 6-8 of the stimulated IVF cycle, second on the day of embryo transfer and the third one day post transfer.
Participants in the comparison group will receive no intervention but will receive standard care.
(3) Measures: The primary outcome measures include prostacyclin and thromboxane vasoactive biomarkers.
Secondary outcome measures include perceived stress levels.
(4) Procedure: Upon IRB approval, an informed consent will be provided to all participants.
Pre- and post- acupuncture urinary metabolites of prostacyclin and thromboxane will be assessed.
A standardized Perceived Stress Scale will be administered before and after each acupuncture session for the study group, and before and after a 30-40-minute waiting period for the control group.
Обзор исследования
Подробное описание
Hypothesis and Specific Aims
The purpose of this pilot study is to determine if acupuncture affects the vasoactive molecules (prostacyclin and thromboxane) in women undergoing IVF therapy. The investigators' overall hypotheses for this area of study, to be addressed with future research, are: (1) acupuncture augments IVF success by enhancing the perfusion of pelvic organs including the ovaries and the uterus, and (2) acupuncture reduces the levels of stress and optimizes mind-body interaction in individuals undergoing IVF.
Specific Aims:
- To measure urine prostacyclin and thromboxane, before and after acupuncture, and
- to assess the impacts of acupuncture on the psychological well-being of women undergoing IVF treatment.
SIGNIFICANCE OF THE STUDY Results from this study will shed light on the mechanism by which acupuncture improves IVF outcomes. This may lead to other treatment strategies to improve success. Likewise, an established mechanism by which acupuncture improves IVF may lead to greater acceptance of this non-conventional treatment modality by the general population.
Research Design and Methods
This is a prospective, randomized, controlled study. Participants will be women in the Principal Investigator's practice seeking IVF. Participants will be randomized 1:1 into either the acupuncture group or the standard of care (no acupuncture) group. Each group will have 3 study visits.
Rationale for the Control Group:
A sham control group is not used because systematic review suggested that sham acupuncture controls may unnecessarily complicate the RCT evidence base given the nature of objective outcomes in IVF study (http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124624/).
Power analysis
With 35 patients allocated to each group, assuming the Student's T-test will be used to determine the differences between two independent samples, effect sizes d>0.6 will be found statistically significant with alpha .05 and power .80. In practical terms, since the PSS validation samples showed a mean about 13.5 with variance=6.2, only averaged differences greater than 1.5 raw score points in PSS will be found statistically significant.
The investigators plan to seek extramural funding in the future. The investigators will use the data obtained from this pilot study to perform power analysis and to calculate the number of participants needed in future proposals.
Тип исследования
Интервенционный
Регистрация (Действительный)
60
Фаза
- Непригодный
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Места учебы
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Texas
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Lubbock, Texas, Соединенные Штаты, 79430
- Texas Tech Health Science Center
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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
От 21 год до 42 года (Взрослый)
Принимает здоровых добровольцев
Да
Полы, имеющие право на обучение
Женский
Описание
Inclusion Criteria:
- Women between ages 21-42 years seeking IVF.
- Willing to undergo acupuncture
- No contraindications to needle insertion.
Exclusion Criteria:
- Women currently using alternative therapies such as acupressure, herbal supplements and meditation techniques.
- Women with generalized psoriasis, neuropathy or coagulopathies posing increased risk due to needle insertion.
- Women with previous experience with acupuncture.
***Please note that we are unable to give a discount on IVF cost for participating in the study.***
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: Фундаментальная наука
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
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Экспериментальный: Acupuncture arm
Participants receiving acupuncture during IVF process
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Participants will receive 3 acupuncture sessions during IVF process
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Без вмешательства: Control
Control arm not receiving acupuncture during IVF process
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Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Urine prostacyclin before and after acupuncture
Временное ограничение: Within 8-week course of IVF treatment
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Measurement of the vasoactive molecule prostacyclin (pg/mg creatinine) in women undergoing IVF therapy.
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Within 8-week course of IVF treatment
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Urine thromboxane before and after acupuncture
Временное ограничение: Within 8-week course of IVF treatment
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Measurement of the vasoactive molecule thromboxane (pg/mg creatinine) in women undergoing IVF therapy.
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Within 8-week course of IVF treatment
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Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Следователи
- Главный следователь: Jennifer L Phy, DO, Texas Tech University Health Sciences Center
Публикации и полезные ссылки
Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.
Общие публикации
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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)
1 ноября 2015 г.
Первичное завершение (Действительный)
1 июля 2020 г.
Завершение исследования (Действительный)
1 сентября 2020 г.
Даты регистрации исследования
Первый отправленный
7 октября 2015 г.
Впервые представлено, что соответствует критериям контроля качества
28 октября 2015 г.
Первый опубликованный (Оценивать)
29 октября 2015 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
16 сентября 2020 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
11 сентября 2020 г.
Последняя проверка
1 сентября 2020 г.
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- L15-117
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. .