Pregnancy With Insomnia: a Trial of Acupuncture (GAS)
Acupuncture is widely used for treatment of insomnia. The research hypothesis is that acupuncture may be more effective than sham acupuncture to treat insomnia during pregnancy.
GAS is a randomized controlled trial with placebo acupuncture using the insomnia severity index (ISI) as the main outcome criterion.
調査の概要
詳細な説明
Scientific justification:
- During pregnancy, insomnia occurs mainly in women without a previous history of sleep disorder, and may remain after delivery. Insomnia affects the quality of life. It might be associated with an increase in labor duration and cesarean section rate.
Insomnia tends to worsen during gestation, owing to back pain, an increased need to micturate, and the movement of the fetus. Sleep disorders are often associated with restless legs syndrome.
- To treat insomnia during pregnancy, the Haute Autorité de Santé (HAS) recommends avoiding using psychotropic medications. It also recommends screening for depression or anxiety traits often associated with insomnia. However, in most cases, psychological means alone fail to treat insomnia effectively.
- Based on 11 randomized controlled trials, the odds of improving sleep disorders are 3 times greater with than without acupuncture, but the methodological quality of these trials is considered insufficient to conclude.
Population:
The study focused on pregnant women suffering from insomnia, excluding women with pregnancies complicated by pre-eclampsia, fetal growth anomalies, or threatened premature labor for fear those complications might interact with sleep disorders, as well as women with known psychiatric disorders. We also excluded women with a history of insomnia before pregnancy to focus on insomnia triggered by pregnancy only.
Objectives:
- Primary objective: To assess the effect of a standardized acupuncture protocol vs. placebo on insomnia during pregnancy.
- Secondary objectives: To assess the effect of a standardized acupuncture protocol vs. placebo on (i) the Pittsburgh Sleep Quality Index (PSQI), (ii) anxiety and depression traits, (iii) use of psychotropic medicines and (iv) recreational substances, (v) the incidence of restless legs syndrome, (vi) perinatal outcome .
Study design:
- Study Type: Multicentre, Interventional, randomized, 2 parallel groups
- Endpoint Classification: Efficacy Study
- Intervention Model: Parallel Assignment
- Masking: Single blind (patient blinded to intervention)
- Primary Purpose: Treatment
- One acupuncture session weekly for 4 consecutive weeks
Visits:
- Selection: When a pregnant woman complains from insomnia, the health professional in charge will fill a checklist of inclusion and exclusion criteria, provide the patient with a pre inclusion ISI questionnaire and give the patient an information sheet and a copy of the consent. When a pregnant woman is sent to the acupuncturist for sleep disorders, he or she may proceed to the selection visit.
- Inclusion: The acupuncturist checks for inclusion and exclusion criteria, collects the patient written consent, performs the clinical examination, gives the corresponding self-assessment questionnaires and proceeds to computerized randomization.
- Follow-up: At visits 1 to 4, the acupuncturist performs the treatment, and records side effects if any. Visits are scheduled on a weekly basis.
- End of research: At visit 5 (one week after last acupuncture session), the acupuncturist gives the corresponding self-assessment questionnaires.
研究の種類
入学 (予想される)
段階
- 適用できない
連絡先と場所
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Age > 18 years
- Singleton pregnancy
- Gestational age ≥ 16 weeks + 0 day and ≤ 32 weeks + 6 days
- Insomnia Severity Index ≥ 10
- Insomnia reported to have started during pregnancy and at least 2 weeks before inclusion
- Patient understanding the study
- Informed consent signed
- Social insurance available at inclusion and until the end of pregnancy
Exclusion Criteria:
- Threatened premature labor
- Small fetus for gestational age
- Pre-eclampsia
- Insomnia starting before pregnancy
- Use of psychotropic drugs before pregnancy
- Use of recreational drugs during pregnancy
- Known psychiatric disorder
- Anticoagulant therapy
- Patient reporting insomnia results from chronic or acute pain
- Obstructive sleep apnea (OSA) requiring treatment
- Patient under antidepressant therapy
- Patient under legal guardianship or deprived of freedom
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的:Regular acupuncture needles
Real acupuncture procedure The real acupuncture will be performed by means of standard stainless-steel needles (0.30-mm diameter, 30-mm length/Gauge 8 x 1.2"), located bilaterally in 5 real acupoints.
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The patient will be in a semi recumbent position during needle penetration.
Duration of needle insertion: 30 minutes
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偽コンパレータ:Sham acupuncture needles
Sham acupuncture with a no penetrating sham needle (blunt and telescopic), giving the impression of insertion but without penetrating the skin will be placed bilaterally in 5 false acupoints
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The patient will be in a semi recumbent position during needle penetration.
Duration of needle insertion: 30 minutes
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Insomnia severity index (ISI)
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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Difference of ISI self-report questionnaire administrated at inclusion visit and 5 weeks after the first acupuncture session
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Inclusion visit and 5 weeks after the first acupuncture session
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Pittsburgh Sleep Quality Index (PSQI)
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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Difference of PSQI self-report questionnaire administrated at inclusion visit and 5 weeks after the first acupuncture session
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Inclusion visit and 5 weeks after the first acupuncture session
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Hospital Anxiety and Depression Scale (HADS)
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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Difference of HADS self-report questionnaire administrated at inclusion visit and 5 weeks after the first acupuncture session
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Inclusion visit and 5 weeks after the first acupuncture session
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Cumulated dose of each psychotropic medicine
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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During the study period, the patients will note on a logbook the daily use of any drug.
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Inclusion visit and 5 weeks after the first acupuncture session
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Cumulated dose of alcohol
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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During the study period, the patients will note on a logbook the daily use of alcohol.
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Inclusion visit and 5 weeks after the first acupuncture session
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Cumulated dose of tobacco
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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During the study period, the patients will note on a logbook the daily use of tobacco.
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Inclusion visit and 5 weeks after the first acupuncture session
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Cumulated dose of cannabis
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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During the study period, the patients will note on a logbook the daily use of cannabis.
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Inclusion visit and 5 weeks after the first acupuncture session
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Cumulated dose of other recreational substances or medicine
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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During the study period, the patients will note on a logbook the daily use of other recreational substances and medicine.
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Inclusion visit and 5 weeks after the first acupuncture session
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Difference in the frequency of restless leg syndrome
時間枠:Inclusion visit and 5 weeks after the first acupuncture session
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According to the guidelines of the International Restless Legs Syndrome Study Group. The diagnosis of restless leg will rely on the presence of all of the following criteria:
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Inclusion visit and 5 weeks after the first acupuncture session
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Perinatal outcome - Gestational age at birth
時間枠:At birth
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The gestational age at birth of the newborn will be recorded.
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At birth
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Perinatal outcome - birth weight
時間枠:At birth
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The weight (in gr) at birth of the newborn will be recorded.
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At birth
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Perinatal outcome - birth height
時間枠:At birth
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The height (in cm) at birth of the newborn will be recorded.
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At birth
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Perinatal outcome - sex
時間枠:At birth
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The sex of the newborn will be recorded.
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At birth
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Perinatal outcome - perinatal mortality
時間枠:At birth
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The perinatal mortality will be recorded.
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At birth
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Perinatal outcome - five minutes Apgar score
時間枠:At birth
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The five minutes Apgar score will be recorded.
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At birth
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Perinatal outcome - cesarean section rate
時間枠:At birth.
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Cesarean section rate will be recorded.
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At birth.
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協力者と研究者
捜査官
- 主任研究者:Stéphanie Nicolian, Midewife、Assistance Publique - Hôpitaux de Paris
研究記録日
主要日程の研究
研究開始 (予想される)
一次修了 (予想される)
研究の完了 (予想される)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
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