LENSのアウトカム予測因子の調査
不安が高まった成人における、解釈の認知バイアス修正(CBM-I)トレーニングであるLENSからの結果予測因子の調査
Anxiety is a very common mental health problem. For people living with anxiety, it can have a huge impact on their lives. There are treatments that can help, such as Cognitive Behavioural Therapy (CBT). However, about half of the people who receive treatment still struggle with anxiety after treatment is complete, and we do not yet know why. In this study, we hope to find factors that help explain why people respond differently to anxiety treatment. To answer this question, people in this study will receive a digital anxiety treatment called Learning Effective New Strategies (LENS). LENS is a type of brain training that helps people make less negative interpretations of uncertain situations and information. LENS has been proven to help reduce worry and anxiety, and improve mood (Hirsch et al., 2021). After participants finish LENS, we will measure how their patterns of thinking and mood changes over treatment and during the following five months. We will invite people to take part through multiple existing research studies (e.g. GLAD, TEDS) who have already shared their genetic data (information about their DNA). This way of recruiting would allow us to combine this genetic data with information from questionnaires to look for genetic and psychological factors that are linked with how well someone's anxiety improves after treatment. This research could help us understand what factors are linked to a person's outcomes from treatment. In the future, this could help health professionals personalise anxiety treatment and offer the right treatment to people sooner. This would mean that fewer people need to try multiple treatments before finding one that works. We hope this study will improve care for people living with anxiety.
調査の概要
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:Colette R Hirsch
- 電話番号:+44 (0) 20 7848 0697
- メール:colette.hirsch@kcl.ac.uk
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
サンプリング方法
調査対象母集団
Participants who have taken part in previous genetic cohort studies, namely GLAD, TEDS and Genes & Health, will be invited to participate in the study.
説明
Inclusion Criteria:
- Adults over the age of 18
- Fluent in English
- Normal or corrected to normal hearing
- Normal or corrected to normal vision
- Currently experiencing anxiety (GAD-7 score ≥ 8)
- Access to stable internet connection
- Access to smartphone, laptop, computer, or tablet
Exclusion Criteria:
- Current high levels of suicidal ideation, as defined by a score ≥ 2 on Item 9 of the PHQ-9 OR score of 1 on Item 9 of the PHQ-9 and score ≥21 on the SIDAS
- Suicide attempt in past two years.
- Current or history of psychosis or bipolar disorder.
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
- 観測モデル:COHORT
- 時間の展望:PROSPECTIVE
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 |
|---|---|---|
|
General Anxiety Disorder-7 score
時間枠:8 week follow up
|
General Anxiety Disorder-7 score on GAD-7 questionnaire |
8 week follow up
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Colette R Hirsch、King's College London
- 主任研究者:Thalia Eley、King's College London
- 主任研究者:Gerome Breen、King's College London
- 主任研究者:Ewan Carr、King's College London
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
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。