A Study of the Effects of a One-session Mindfulness of the Breath Meditation Practice on State Hope and State Gratitude in the General Population

Sponsor
Canterbury Christ Church University (Other)
Overall Status
Completed
CT.gov ID
NCT04099758
Collaborator
(none)
580
1
2
8.6
67.4

Study Details

Study Description

Brief Summary

This study aims to examine whether a brief mindfulness of the breath meditation practice is more helpful than listening to an audio recording in relation to improving hope and gratitude in the general population.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness of the breath meditation
  • Behavioral: Audio-recording control
N/A

Detailed Description

This one-session online study will randomise members of the general public to either 1) a mindfulness of the breath meditation practice lasting 10 minutes or 2) an audio-recording control of the same length. State measures of mindfulness, hope and gratitude will be taken immediately before (baseline) and after the intervention/control. In addition, the study will also measure trait mindfulness at baseline.The primary hypothesis is that engaging in a brief mindfulness practice will result in beneficial changes in state hope compared to control. Other hypotheses are that: engaging in a brief mindfulness practice will result in beneficial changes in state gratitude compared to control; that the effect of mindfulness practice on state hope will be statistically mediated by change in state mindfulness; that the effect of mindfulness practice on state gratitude will be statistically mediated by change in state mindfulness; and that baseline trait mindfulness will statistically moderate the effect of mindfulness practice on change in state mindfulness in the above mentioned mediation models (i.e. that moderated mediation will be observed).

Study Design

Study Type:
Interventional
Actual Enrollment :
580 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized controlled study.Randomized controlled study.
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
Participants will be randomised and complete the study, including outcome measures, through an automated online programme, without involvement of the researcher.
Primary Purpose:
Basic Science
Official Title:
One-session Mindfulness of the Breath Meditation Practice: A Randomized Controlled Study of the Effects on State Hope and State Gratitude
Actual Study Start Date :
Oct 28, 2019
Actual Primary Completion Date :
Jul 16, 2020
Actual Study Completion Date :
Jul 16, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mindfulness of the breath meditation

10 minute mindfulness of the breath meditation practice delivered online via audio-recording.

Behavioral: Mindfulness of the breath meditation
A 10-minute mindfulness of the breath meditation practice

Placebo Comparator: Audio-recording control

10 minute non-fiction audio-recording delivered online

Behavioral: Audio-recording control
10 minute non-fiction audio-recording delivered online

Outcome Measures

Primary Outcome Measures

  1. Change from baseline to post-intervention on the State Hope Scale (SHS). [Baseline (0 minutes), post-intervention (10 minutes).]

    The SHS is a 6-item self-report measure of state hope. The total score on SHS ranges from 8 to 48 , with higher score indicating greater state hope.

Secondary Outcome Measures

  1. Change from baseline to post-intervention on the Gratitude Adjective Checklist (GAC). [Baseline (0 minutes), post-intervention (10 minutes).]

    The GAC is a 3-item self-report measure of state gratitude. The total score on GAC ranges from 3 to 15, with higher score indicating greater state gratitude.

Other Outcome Measures

  1. Change from baseline to post-intervention on the Toronto Mindfulness Scale (TMS). [Baseline (0 minutes), post-intervention (10 minutes).]

    The TMS is a 13-item self-report measure of state mindfulness that produces scores for curiosity and decentering. The curiosity score ranges from 0 to 24, the decentering score from 0 to 28, and the total score from 0 to 52, with higher scores indicating greater curiosity, decentering and overall state mindfulness respectively.

  2. Five Factor Mindfulness Questionnaire -15 item version (FFMQ-15) [Baseline (0 minutes)]

    The FFMQ-15 is a 15-item measure of trait mindfulness. It will be administered at baseline only. The total score on the FFMQ-15 ranges from 15 to 75, with higher score indicating greater trait mindfulness. (Note that the observe subscale will be excluded from the calculation of the total score, as recommended in https://doi.org/10.1002/jclp.21865 and http://dx.doi.org/10.1037/pas0000263 producing a total score between 12 and 60).

  3. Bespoke manipulation check questionnaire. [Post-intervention (10 minutes)]

    Participants rate the extent to which they paid attention during the intervention and followed the guidance on 0 - 10 scales, with higher scores indicating greater compliance.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Members of the general public.

  • Adequate understanding of spoken and written English.

  • Internet access.

Exclusion Criteria:

-Currently experiencing very severe problems with their mental health.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Canterbury Christ Church University Tunbridge Wells Kent United Kingdom TN1 2YG

Sponsors and Collaborators

  • Canterbury Christ Church University

Investigators

  • Principal Investigator: Sarah Strohmaier, BA, MSc, Canterbury Christ Church University
  • Study Director: Fergal Jones, PhD, PsychD, Canterbury Christ Church University
  • Study Director: James Cane, PhD, Canterbury Christ Church University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Canterbury Christ Church University
ClinicalTrials.gov Identifier:
NCT04099758
Other Study ID Numbers:
  • S_Strohmaier_22_07_2019
First Posted:
Sep 23, 2019
Last Update Posted:
Aug 24, 2020
Last Verified:
Sep 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 24, 2020