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Clinical Trials/NCT04674124
NCT04674124CompletedNot Applicable

Feasibility and Acceptability of an Online Mindfulness-based Intervention for Mothers Within the Postpartum Period

Canterbury Christ Church University1 site in 1 country112 target enrollmentStarted: December 13, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
112
Locations
1
Primary Endpoint
Differences in scores between groups at post intervention (10) and follow up (14) on the Short Warwick-Edinburgh Mental Well-Being Scale

Study Overview

Brief Summary

This research study is aiming to explore whether an online mindfulness programme is accessible and supportive for first time mothers who has a child who is less than 12 months old.

Detailed Description

This study is a randomised controlled trial (RCT) comparing an online mindfulness based course (10ofZen) with a treatment as usual group (delayed 10ofZen course materials). Participants will be informed about the study and asked to undertake a screening questionnaire to ensure the eligibility criteria is met. Following this, participants will be invited to give online consent. A battery of self-report measures will be administered online at baseline (week 0), post-intervention (week 10) and at follow-up (week 14). A sleep measure will also be undertaken and used as a co-variate during data analysis. At the end of participation in the research study, all participants will gain access to the course materials, including audio recordings of meditations and any written materials used within the course.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Women who identify as a mother (Biological, adoptive, foster-carer or step-mum)
  • •Have an infant under the age of 12 months at baseline measures
  • •Sufficient English reading and listening abilities
  • •Access to the internet via an electronic device (phone, tablet, laptop or computer)
  • •Access to a mobile phone
  • •No prior experience of parenting a baby (under 12 months of age)

Exclusion Criteria

  • •Previous completion of a formal 8-week mindfulness course or current mindfulness/meditation practice
  • •Currently pregnant
  • •Severe levels of depression and/or anxiety as measured by 15+ point on the Generalised Anxiety Disorder-7 and Patient Health Questionnaire-9 (NICE, 2011).
  • •Suicidal ideation or thoughts of self-harm in the last two weeks
  • •Currently experiencing symptoms of psychosis
  • •Diagnosis of Post Traumatic Stress Disorder (PTSD)
  • •Bereavement within the last six months which they still feel affected by.

Arms & Interventions

Online Mindfulness Course

Experimental

Participants will be enrolled on a 9 week online mindfulness course.

Intervention: Brief Online Mindfulness Intervention (Behavioral)

Delayed course materials

No Intervention

Participants will have access to the course materials at the closure of their involvement in the study.

Outcomes

Primary Outcomes

Differences in scores between groups at post intervention (10) and follow up (14) on the Short Warwick-Edinburgh Mental Well-Being Scale

Time Frame: Post-intervention and follow up ( i.e 10 & 14 weeks post baseline)

Self-report measure of perceived well-being. Scores can range from 0-35. Higher scores are indicative of higher levels of subjective wellbeing.

Secondary Outcomes

  • Differences in scores between groups at post intervention (10) and follow up (14) on the Maternal Postnatal Attachment Scale(Post-intervention ( i.e 10 & 14 weeks post baseline))
  • Differences in scores between groups at post intervention (10) and follow up (14) on the Depression Anxiety Stress Scale - 21(Post-intervention ( i.e 10 & 14 weeks post baseline))
  • Differences in scores between groups at post intervention (10) and follow up (14) Five Facet Mindfulness Questionnaire - 15(Post-intervention ( i.e 10 & 14 weeks post baseline))
  • Differences in scores between groups at post intervention (10) and follow up (14) on sleep quality(Post-intervention ( i.e 10 & 14 weeks post baseline))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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