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Digital Cognitive Behavioral Therapy (dCBT-I) for Maternal Insomnia

Primary Purpose

Digital Cognitive Behavioral Therapy for Insomnia (dCBT-I)

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
dCBT-I
Sponsored by
Women's Hospital School Of Medicine Zhejiang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Digital Cognitive Behavioral Therapy for Insomnia (dCBT-I)

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-40 years old
  • 20-32 weeks of pregnancy, singleton pregnancy and regular obstetric examination at Zhejiang University Women's Hospital
  • There has been a high frequency of insomnia symptoms
  • According to the preliminary assessment by the project team, it meets the diagnostic criteria for insomnia
  • Possess a smart phone and can operate it proficiently, with normal reading and writing comprehension ability, clear consciousness, and able to cooperate with the research to complete the questionnaire independently.

Exclusion Criteria:

  • Assess the risk of preterm birth and concurrent pregnancy-related diseases;
  • Completion of the 7-day sleep diary in the baseline period < 4 days;
  • Combined with severe anxiety/depression;
  • Suicidal tendencies or severe mental illness (bipolar disorder, schizophrenia, paranoid psychosis, etc.);
  • Edinburgh Pregnancy Depression Scale (EPDS) total score ≥ 15;
  • Have drug dependence or have taken anti-anxiety, anti-depression, sedative or hypnotic drugs for mental diseases within the past 3 months;
  • Participated in interventions such as meditation courses, childbirth yoga or cognitive behavioral therapy in the past 1 year;
  • Complicated with serious physical diseases such as heart failure and tumor;
  • Combined with sleep disorders such as severe obstructive sleep apnea that require further evaluation and treatment;
  • There is alcohol and cigarette dependence;
  • Shift work;
  • Severe visual or hearing impairment and unable to use mobile phones normally;
  • Physical illness with unstable condition, or illness itself that may interfere with cognitive behavioral therapy for insomnia.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    dCBT-I treatment group

    Arm Description

    Outcomes

    Primary Outcome Measures

    Change of "Insomnia Severity Index(ISI)"
    Insomnia Severity Index(ISI),the minimum and maximum values are 0 and 28, and higher scores mean a worse outcome.

    Secondary Outcome Measures

    Change of "Pittsburgh Sleep Quality Index(PSQI)"
    Pittsburgh Sleep Quality Index(PSQI),the minimum and maximum values are 0 and 21, and higher scores mean a worse outcome.
    Change of "sleep onset latency(SOL)"
    simple questionnaire will be used to assess this outcome of sleep onset latency(SOL)
    Change of "wake up after sleep onset(WASO)"
    simple questionnaire will be used to assess this outcome of WASO
    Change of "sleep efficiency(SE)"
    combination of questionnaire and calculate will be used to assess this outcome of SE
    Change of "Number of wake ups during the night"
    Number of wake ups during the night
    Change of "total sleep time(TST)"
    total sleep time(TST)
    Change of "Edinburgh Pregnancy Depression Scale(EPDS)"
    Edinburgh Pregnancy Depression Scale(EPDS),the minimum and maximum values are 0 and 30, and higher scores mean a worse outcome.
    Change of "Self-rating Anxiety Scale(SAS)"
    Self-rating Anxiety Scale(SAS), the minimum and maximum values are 25 and 100, and higher scores mean a worse outcome.

    Full Information

    First Posted
    May 16, 2022
    Last Updated
    May 24, 2022
    Sponsor
    Women's Hospital School Of Medicine Zhejiang University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05395546
    Brief Title
    Digital Cognitive Behavioral Therapy (dCBT-I) for Maternal Insomnia
    Official Title
    Digital Cognitive Behavioral Therapy (dCBT-I) for Maternal Insomnia During Pregnancy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    June 1, 2022 (Anticipated)
    Primary Completion Date
    July 15, 2022 (Anticipated)
    Study Completion Date
    June 1, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Women's Hospital School Of Medicine Zhejiang University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    Insomnia symptoms are common during pregnancy, especially in the second and third trimesters, which can reach more than 68%. Insomnia during pregnancy is not only associated with increased risk of preeclampsia, gestational diabetes, preterm labor, and cesarean section, but also increased postpartum poor sleep and postpartum depression. Cognitive behavioral therapy (CBT-I) and drug therapy for insomnia are the two main methods of insomnia treatment. Drug therapy is the more commonly used traditional treatment method, but there may be certain drug risks. Therefore, non-drug methods for Insomnia in pregnant women is much safer. Cognitive-behavioral therapy for insomnia is a psychological therapy for insomnia. Compared with sedative-hypnotic drugs, its therapeutic effect is slow, but the curative effect is long-lasting, with less relapse after treatment and no invasive side effects. Multiple guidelines recommend it as first-line therapy for insomnia. And "Digital Cognitive Behavioral Therapy" (dCBT-I), is based on CBT-I, a therapy provided by the Internet and smartphones, which simulates face-to-face CBT-I in reality. It can provide more convenient medical services for the special group of pregnant women, improve sleep, improve mental symptoms, life treatment, and reduce the risk of adverse outcomes for mothers and children. The Womens' Hospital, Zhejiang University School of Medicine is conducting a clinical study on "Digital Cognitive Behavioral Therapy (dCBT-I) for maternal Insomnia during pregnancy". The primary goal of this research project was to examine the efficacy of dCBT-I ("RuMian") in the treatment of maternal insomnia. "RuMian" is a fully automatic dCBT-I application developed in China, and subjects will use it for free.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Digital Cognitive Behavioral Therapy for Insomnia (dCBT-I)

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    dCBT-I treatment group
    Arm Type
    Experimental
    Intervention Type
    Other
    Intervention Name(s)
    dCBT-I
    Other Intervention Name(s)
    Device: smartphone
    Intervention Description
    Complete the evaluation of various scales and record a 7-day sleep diary before entering the group Receive a 6-week treatment after enrollment, insist on using the app every day (about 5-10 minutes), and receive regular follow-up from the project doctor Scale assessment needs to be completed at the end of treatment One month after the end of treatment, cooperate with relevant follow-up and complete the scale evaluation
    Primary Outcome Measure Information:
    Title
    Change of "Insomnia Severity Index(ISI)"
    Description
    Insomnia Severity Index(ISI),the minimum and maximum values are 0 and 28, and higher scores mean a worse outcome.
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Secondary Outcome Measure Information:
    Title
    Change of "Pittsburgh Sleep Quality Index(PSQI)"
    Description
    Pittsburgh Sleep Quality Index(PSQI),the minimum and maximum values are 0 and 21, and higher scores mean a worse outcome.
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Title
    Change of "sleep onset latency(SOL)"
    Description
    simple questionnaire will be used to assess this outcome of sleep onset latency(SOL)
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Title
    Change of "wake up after sleep onset(WASO)"
    Description
    simple questionnaire will be used to assess this outcome of WASO
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Title
    Change of "sleep efficiency(SE)"
    Description
    combination of questionnaire and calculate will be used to assess this outcome of SE
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Title
    Change of "Number of wake ups during the night"
    Description
    Number of wake ups during the night
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Title
    Change of "total sleep time(TST)"
    Description
    total sleep time(TST)
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Title
    Change of "Edinburgh Pregnancy Depression Scale(EPDS)"
    Description
    Edinburgh Pregnancy Depression Scale(EPDS),the minimum and maximum values are 0 and 30, and higher scores mean a worse outcome.
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)
    Title
    Change of "Self-rating Anxiety Scale(SAS)"
    Description
    Self-rating Anxiety Scale(SAS), the minimum and maximum values are 25 and 100, and higher scores mean a worse outcome.
    Time Frame
    From before treatment to the end of treatment (an average of 42 days)

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age 18-40 years old 20-32 weeks of pregnancy, singleton pregnancy and regular obstetric examination at Zhejiang University Women's Hospital There has been a high frequency of insomnia symptoms According to the preliminary assessment by the project team, it meets the diagnostic criteria for insomnia Possess a smart phone and can operate it proficiently, with normal reading and writing comprehension ability, clear consciousness, and able to cooperate with the research to complete the questionnaire independently. Exclusion Criteria: Assess the risk of preterm birth and concurrent pregnancy-related diseases; Completion of the 7-day sleep diary in the baseline period < 4 days; Combined with severe anxiety/depression; Suicidal tendencies or severe mental illness (bipolar disorder, schizophrenia, paranoid psychosis, etc.); Edinburgh Pregnancy Depression Scale (EPDS) total score ≥ 15; Have drug dependence or have taken anti-anxiety, anti-depression, sedative or hypnotic drugs for mental diseases within the past 3 months; Participated in interventions such as meditation courses, childbirth yoga or cognitive behavioral therapy in the past 1 year; Complicated with serious physical diseases such as heart failure and tumor; Combined with sleep disorders such as severe obstructive sleep apnea that require further evaluation and treatment; There is alcohol and cigarette dependence; Shift work; Severe visual or hearing impairment and unable to use mobile phones normally; Physical illness with unstable condition, or illness itself that may interfere with cognitive behavioral therapy for insomnia.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Zhaoxia Liang
    Phone
    +860571-87061501
    Email
    xiaozaizai@zju.edu.cn

    12. IPD Sharing Statement

    Learn more about this trial

    Digital Cognitive Behavioral Therapy (dCBT-I) for Maternal Insomnia

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