Text Messaging to Improve HIV Testing Among Young Women in Kenya (T2T)
Evaluating Feasibility and Potential Impact of Text Messages on HIV Awareness Among Young Women in Rural Kenya: a Pilot Study
調査の概要
詳細な説明
In Kenya, women have higher rates of infection (6.9%) than men (4.4%) and young women aged 15-24 years are over three times more likely to be infected than young men of the same age group. HIV testing and counseling remains critical to identifying new infections and preventing the spread of HIV but many young women do not test and still continue to engage in high risk behavior.
HIV programs have begun to leverage mobile phones and text messages to increase the reach and scale of interventions. Kenya currently has 32.2 million mobile phone subscribers, representing a 79.2% country penetration. Text messages have been used successfully in Kenya for marketing purposes and have even been demonstrated to increase antiretroviral (ART) adherence. Despite advances in mobile-based applications to improve issues in health, none of these health applications have yet been able to reach the scale of mobile phone-based financial products in Kenya.
Given the potential synergies of text message use and need for HIV testing, a randomized quasi-experimental study was conducted to test whether weekly text messages encouraging HIV testing and improving HIV awareness would increase HIV testing, enhance HIV risk perception and reduce high risk behaviour among young women 18-24 years old in a predominantly rural region in Kenya.
Women in the intervention arm received access to a suite of HIV sensitization text messages sent weekly to increase their awareness of HIV and encourage them to test with the option of texting back for more information to a maximum of three times per week. Women in the control arm did not receive these messages. All women were followed up for six months with monthly SMS surveys collecting data on their HIV testing practices, sexual behaviour and risk perception.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Nairobi、ケニア、00202
- Partners in Health and Research Development (Phrd)
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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:
- Own a mobile phone which they don't share and which operates on a telecom provider supported by our SMS platform
- Be HIV uninfected (by self report) or not know their HIV status
- Report not having tested for HIV in the preceding 12 months
- Know how to send and receive SMS
- Must consent to the study
- Have regular access to electricity for charging a cell phone
Exclusion Criteria:
- Did not consent to the study
- Did not meet inclusion criteria
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:防止
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
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:Behavioural
Intervention arm receiving weekly HIV sensitization text messages
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Weekly HIV sensitization text messages with option to text back up to 3 times per week for additional messages.
Message topics included pregnancy, condoms, sexually transmitted infections, contraceptives, anal sex and personal risk of HIV.
All messages ended with the phrase "Get tested for HIV".
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介入なし:Control
No weekly messages were sent to this group
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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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First HIV test
時間枠:End of study (6 months after enrollment)
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Time to first reported HIV test will be compared between the two study arms
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End of study (6 months after enrollment)
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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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Reported sexual behaviour patterns
時間枠:End of study (6 months after enrollment)
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Sexual behaviour data (number of new sexual partners, concurrent sexual partnerships and number of sex acts where condoms are used) was collected via a text message survey monthly during study follow up and responses will be compared between the two study arms
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End of study (6 months after enrollment)
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Self perception of risk
時間枠:End of study (6 months after enrollment)
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Self perception of HIV risk in both arms will be compared against HIV testing habits and sexual partnerships
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End of study (6 months after enrollment)
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協力者と研究者
スポンサー
協力者
捜査官
- 主任研究者:Njambi Njuguna, MBChB,MPH、University of Washington; Kenyatta National Hospital
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
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 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
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。