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Enjoy Your Bump : Online Cognitive Behavioural Therapy in Pregnancy

Primary Purpose

Perinatal Mental Health, Antenatal Depression, Antenatal Anxiety

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Enjoy Your Bump
Sponsored by
University of Edinburgh
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional health services research trial for Perinatal Mental Health focused on measuring Online Cognitive Behavioural Therapy, Pregnancy, Self-help

Eligibility Criteria

18 Years - 55 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Singleton pregnancy
  • Mild-moderate chronic perinatal mental health identified by a score of 2 or higher on PHQ-2 and/or GAD-2.
  • 16+0 to 32+6 weeks at recruitment

Exclusion Criteria:

  • Severe perinatal mental health problem such as schizophrenia, bipolar disorder, substance abuse/dependence, active risk of self-harm.
  • Already receiving psychological therapy.
  • Insufficient English language to engage with intervention or complete questionnaires.
  • Unable to give informed consent.
  • Illiterate
  • No internet access
  • Taking part in another current research project focused on mental health.

Sites / Locations

  • NHS Lothian / University of EdinburghRecruiting

Outcomes

Primary Outcome Measures

Evaluation of recruitment and retention.
Evaluate how many women are recruited to the study, how many women complete the online modules and how many women give feedback on their experience via an online questionnaire.
Evaluation of feedback questionnaire data.
Evaluate the qualitative feedback women give regarding their experience of the intervention using an online questionnaire.
Estimation of effect size for changes in depression.
Obtain an estimate of effect size for changes in depression, from pre to post intervention. Change in effect size for depression will be measured using Standardised Mean Difference (SMD) of scores on Patient Health Questionnaire-9 (PHQ-9) from pre to post intervention.
Estimate of Effect Size for changes in depression (2)
Obtain an estimate of effect size for changes in depression, from pre to post intervention. Change in effect size for depression will be measured using Standardised Mean Difference (SMD) of scores on the Warwick Edinburgh Mental Wellbeing Scale (WEMWBS) from pre to post intervention.
Estimate of effect size for changes in depression (3)
Obtain an estimate of effect size for changes in depression, from pre to post intervention. Change in effect size for depression will be measured using Standardised Mean Difference (SMD) of scores on the Edinburgh Postnatal Depression Score (EPDS) from pre to post intervention.
Estimation of effect size for changes in anxiety.
Effect size for Anxiety will be measured using SMD for Generalised Anxiety-7 questionnaire scores before and after intervention.
Estimation of effect size for changes in social function.
Effect size for social function will be measured using SMD for score on pregnancy experience scale (PES) pre and post intervention.
Estimation of effect size for changes in attachment.
Effect size in attachment will be measured using SMD for scores on Prenatal Attachment Inventory both before and after intervention.

Secondary Outcome Measures

Depression score (1)
Measure depression pre and post intervention using a standardised assessment tool: Patient Health Questionnaire-9 (PHQ-9). This standardised questionnaire measures depression. Score ranges 0-27 with 0 representing least depressed and 27 representing most depressed.
Depression score (2)
Measure depression pre and post intervention using standardised assessment tool: Edinburgh Postnatal Depression Score (EPDS). Another standardised questionnaire. Scores range from 0-30. '0' represents least depressed and '30' represents most depressed.
Depression score (3)
Measure depression pre and post intervention using standardised assessment tool: . Warwick Edinburgh Mental Wellbeing Scale (WEMWS). Another standardised assessment of mood. Scores range from 14 - 70. '14' represents most depressed and '70' represents least depressed.
Anxiety score
Measure anxiety pre and post intervention using standardised assessment tool Generalised Anxiety Disorder-7 Item scale (GAD-7). This standardised questionnaire gives a score between '0-21'. '0' represents the least anxious and '21' represents the most anxious.
Pregnancy Experience
Measure pregnancy experience pre and post intervention using the Pregnancy Experience Scale (PES). This 41-item questionnaire measures participants feelings towards social issues related to their pregnancy. Total score ranges from 0-123. '0' represents no negative feelings towards experience in pregnancy and '123' represents maximum negative experience towards experience of pregnancy.
Measure mother-baby relationship (Antenatal)
Evaluate the mother-baby attachment in the antenatal period pre and post intervention using the Prenatal Attachment Inventory (PAI) The Prenatal Attachment Inventory is a 21-item questionnaire with scores ranging from 21-84 with '21' representing most attached and '84' the least attached.
Measure mother-baby relationship (Postnatal)
Evaluate the mother-baby attachment post intervention in the postnatal period using The Maternal Attachment Inventory (MAI). The Maternal Attachment Inventory is a 26-item questionnaire. Total ranges from '26-104'. 26 represents poor attachment and 104 represents good attachment.
Time taken to complete intervention (1)
Quantify how long it typically takes participants to complete the intervention. This will be assessed in 'minutes participant spent active using the intervention'. This data in recorded on the online programme for researcher to see. We will also measure in weeks, how long it took participants to complete all 5 modules of the Enjoy Your Bump intervention.
Time taken to complete intervention (2).
Quantify how long it typically takes participants to complete the intervention. We will measure in weeks and days, how long it took participants to complete all 5 modules of the Enjoy Your Bump intervention from recruitment date.
Delivery and support of intervention
Test and evaluate the ability to deliver and support the intervention. This will be measured by asking participants in the evaluation questionnaire to comment on how they evaluated the support they received.

Full Information

First Posted
October 11, 2017
Last Updated
December 13, 2017
Sponsor
University of Edinburgh
Collaborators
Edinburgh & Lothians Health Foundation, Tommy's Edinburgh Maternal & Fetal Health Centre, National Health Service (NHS) Lothian, Five Areas Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT03373734
Brief Title
Enjoy Your Bump : Online Cognitive Behavioural Therapy in Pregnancy
Official Title
Feasibility Study Investigating the Efficacy and Acceptability of a Pregnancy Focussed Online Cognitive Behavioural Therapy Package: Enjoy Your Bump
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
May 31, 2017 (Actual)
Primary Completion Date
March 1, 2019 (Anticipated)
Study Completion Date
March 1, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Edinburgh
Collaborators
Edinburgh & Lothians Health Foundation, Tommy's Edinburgh Maternal & Fetal Health Centre, National Health Service (NHS) Lothian, Five Areas Ltd

4. Oversight

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

5. Study Description

Brief Summary
A feasibility study evaluating how acceptable women experiencing low mood or anxiety during their pregnancy find an online Cognitive Behavioural Therapy course called 'Enjoy Your Bump'. This project will also begin to explore the effectiveness of this programme as a low intensity self-help intervention for mild to moderate depressive symptoms during pregnancy.
Detailed Description
'Enjoy Your Bump (EYB)' is an online life skills course based on Cognitive Behavioural Therapy (CBT) principles which has been designed to specifically support women in the antenatal period. A survey of women and health professionals has demonstrated that this is a resource that both groups find acceptable. The aim of this quasi-experimental feasibility study is to evaluate the user experience and efficacy of this online programme as a non-pharmacological, low intensity intervention for women experiencing mild-moderate depressive symptoms in pregnancy. This will be achieved by measuring depression and anxiety as well as measures of attachment to the developing baby, pre and post intervention. It is hoped the results from this study will help inform whether this is a resource that should be made more widely available to women in the National Health Service (NHS). It is hypothesised that the 'Enjoy Your Bump' will be an acceptable and effective intervention for women experiencing mild to moderate depressive symptoms in the antenatal period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Perinatal Mental Health, Antenatal Depression, Antenatal Anxiety
Keywords
Online Cognitive Behavioural Therapy, Pregnancy, Self-help

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Enjoy Your Bump is an online life skills course based on cognitive behavioural therapy principles. It has been designed to address issues pertinent to mood in pregnancy. The course compiles five modules delivered in the form of an online slideshow with audio. It can be accessed from a range of devices. There are a series of worksheets the user can access and download which accompany the modules.
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Enjoy Your Bump
Other Intervention Name(s)
Five Areas Ltd Enjoy Your Bump
Intervention Description
Online life skills course based on Cognitive Behavioural Therapy Principles.
Primary Outcome Measure Information:
Title
Evaluation of recruitment and retention.
Description
Evaluate how many women are recruited to the study, how many women complete the online modules and how many women give feedback on their experience via an online questionnaire.
Time Frame
Measured at 12 months post study start date
Title
Evaluation of feedback questionnaire data.
Description
Evaluate the qualitative feedback women give regarding their experience of the intervention using an online questionnaire.
Time Frame
Measured at 12 months post study start date
Title
Estimation of effect size for changes in depression.
Description
Obtain an estimate of effect size for changes in depression, from pre to post intervention. Change in effect size for depression will be measured using Standardised Mean Difference (SMD) of scores on Patient Health Questionnaire-9 (PHQ-9) from pre to post intervention.
Time Frame
Measured at 12 months post study start date.
Title
Estimate of Effect Size for changes in depression (2)
Description
Obtain an estimate of effect size for changes in depression, from pre to post intervention. Change in effect size for depression will be measured using Standardised Mean Difference (SMD) of scores on the Warwick Edinburgh Mental Wellbeing Scale (WEMWBS) from pre to post intervention.
Time Frame
Measured at 12 months post study start date.
Title
Estimate of effect size for changes in depression (3)
Description
Obtain an estimate of effect size for changes in depression, from pre to post intervention. Change in effect size for depression will be measured using Standardised Mean Difference (SMD) of scores on the Edinburgh Postnatal Depression Score (EPDS) from pre to post intervention.
Time Frame
Measured at 12 months post study start date.
Title
Estimation of effect size for changes in anxiety.
Description
Effect size for Anxiety will be measured using SMD for Generalised Anxiety-7 questionnaire scores before and after intervention.
Time Frame
Measured at 12 months post study start date.
Title
Estimation of effect size for changes in social function.
Description
Effect size for social function will be measured using SMD for score on pregnancy experience scale (PES) pre and post intervention.
Time Frame
Measured at 12 months post study start date.
Title
Estimation of effect size for changes in attachment.
Description
Effect size in attachment will be measured using SMD for scores on Prenatal Attachment Inventory both before and after intervention.
Time Frame
Measured at 12 months post study start date.
Secondary Outcome Measure Information:
Title
Depression score (1)
Description
Measure depression pre and post intervention using a standardised assessment tool: Patient Health Questionnaire-9 (PHQ-9). This standardised questionnaire measures depression. Score ranges 0-27 with 0 representing least depressed and 27 representing most depressed.
Time Frame
Scores will be recorded at recruitment to study (between 16 - 32+6 weeks gestation), Post Enjoy Your Bump Intervention (before 38 weeks gestation) and 12 weeks Postnatal.
Title
Depression score (2)
Description
Measure depression pre and post intervention using standardised assessment tool: Edinburgh Postnatal Depression Score (EPDS). Another standardised questionnaire. Scores range from 0-30. '0' represents least depressed and '30' represents most depressed.
Time Frame
Scores will be recorded at recruitment to study (between 16 - 32+6 weeks gestation), Post Enjoy Your Bump Intervention (before 38 weeks gestation) and 12 weeks Postnatal.
Title
Depression score (3)
Description
Measure depression pre and post intervention using standardised assessment tool: . Warwick Edinburgh Mental Wellbeing Scale (WEMWS). Another standardised assessment of mood. Scores range from 14 - 70. '14' represents most depressed and '70' represents least depressed.
Time Frame
Scores will be recorded at recruitment to study (between 16 - 32+6 weeks gestation), Post Enjoy Your Bump Intervention (before 38 weeks gestation) and 12 weeks Postnatal.
Title
Anxiety score
Description
Measure anxiety pre and post intervention using standardised assessment tool Generalised Anxiety Disorder-7 Item scale (GAD-7). This standardised questionnaire gives a score between '0-21'. '0' represents the least anxious and '21' represents the most anxious.
Time Frame
Scores will be recorded at recruitment to study (between 16 - 32+6 weeks gestation), Post Enjoy Your Bump Intervention (before 38 weeks gestation) and 12 weeks Postnatal.
Title
Pregnancy Experience
Description
Measure pregnancy experience pre and post intervention using the Pregnancy Experience Scale (PES). This 41-item questionnaire measures participants feelings towards social issues related to their pregnancy. Total score ranges from 0-123. '0' represents no negative feelings towards experience in pregnancy and '123' represents maximum negative experience towards experience of pregnancy.
Time Frame
Scores will be recorded at recruitment to study (between 16 - 32+6 weeks gestation), Post Enjoy Your Bump Intervention (before 38 weeks gestation)
Title
Measure mother-baby relationship (Antenatal)
Description
Evaluate the mother-baby attachment in the antenatal period pre and post intervention using the Prenatal Attachment Inventory (PAI) The Prenatal Attachment Inventory is a 21-item questionnaire with scores ranging from 21-84 with '21' representing most attached and '84' the least attached.
Time Frame
Scores will be recorded at recruitment to study (between 16 - 32+6 weeks gestation), and Post Enjoy Your Bump Intervention (before 38 weeks gestation)
Title
Measure mother-baby relationship (Postnatal)
Description
Evaluate the mother-baby attachment post intervention in the postnatal period using The Maternal Attachment Inventory (MAI). The Maternal Attachment Inventory is a 26-item questionnaire. Total ranges from '26-104'. 26 represents poor attachment and 104 represents good attachment.
Time Frame
Score recorded at 12 weeks postnatal
Title
Time taken to complete intervention (1)
Description
Quantify how long it typically takes participants to complete the intervention. This will be assessed in 'minutes participant spent active using the intervention'. This data in recorded on the online programme for researcher to see. We will also measure in weeks, how long it took participants to complete all 5 modules of the Enjoy Your Bump intervention.
Time Frame
Data will be recorded at participant completion of Enjoy Your Bump intervention. Participants are required to complete intervention before they are 38+0 weeks pregnant.
Title
Time taken to complete intervention (2).
Description
Quantify how long it typically takes participants to complete the intervention. We will measure in weeks and days, how long it took participants to complete all 5 modules of the Enjoy Your Bump intervention from recruitment date.
Time Frame
Data will be recorded at participant completion of Enjoy Your Bump intervention. Participants are required to complete intervention before they are 38+0 weeks pregnant.
Title
Delivery and support of intervention
Description
Test and evaluate the ability to deliver and support the intervention. This will be measured by asking participants in the evaluation questionnaire to comment on how they evaluated the support they received.
Time Frame
Data will be recorded at participant completion of Enjoy Your Bump intervention. Participants are required to complete intervention before they are 38+0 weeks pregnant.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Singleton pregnancy Mild-moderate chronic perinatal mental health identified by a score of 2 or higher on PHQ-2 and/or GAD-2. 16+0 to 32+6 weeks at recruitment Exclusion Criteria: Severe perinatal mental health problem such as schizophrenia, bipolar disorder, substance abuse/dependence, active risk of self-harm. Already receiving psychological therapy. Insufficient English language to engage with intervention or complete questionnaires. Unable to give informed consent. Illiterate No internet access Taking part in another current research project focused on mental health.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rebecca M Reynolds, PHD
Phone
01312426762
Email
R.Reynolds@ed.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Fiona C Denison, Reader
Phone
01312426449
Email
Fiona.denison@ed.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rebecca M Reynolds, PHD
Organizational Affiliation
University of Edinburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
NHS Lothian / University of Edinburgh
City
Edinburgh
State/Province
Scotland
ZIP/Postal Code
EH16 4TJ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rebecca M Reynolds, PHD
Phone
01312426762
Email
R.Reynolds@ed.ac.uk
First Name & Middle Initial & Last Name & Degree
Fiona C Denison, Reader
Phone
01312426449
Email
Fiona.Denison@ed.ac.uk
First Name & Middle Initial & Last Name & Degree
Clare M Wallace, MSc

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.eyp.llttf4.com
Description
Enjoy Your Bump home page. As site still under evaluation - requires unique code to access content.

Learn more about this trial

Enjoy Your Bump : Online Cognitive Behavioural Therapy in Pregnancy

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