The effect of a centering meditation on resilience, mindfulness, stress, and hope among college students

ISRCTN ISRCTN13587045
DOI https://doi.org/10.1186/ISRCTN13587045
Secondary identifying numbers EDIRC-2020-08-02-14426-sdorais
Submission date
08/08/2021
Registration date
14/08/2021
Last edited
12/04/2022
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English Summary

Background and study aims
This study aims to examine the effectiveness and dynamic mechanisms of centering meditation in relation to resilience, mindfulness, stress, spiritual transcendence, and hop over a span of time. This study consists of two primary aims: 1) to determine the effectiveness of centering prayer on increasing resilience, stress, mindfulness, and hope and 2) to examine the temporal dynamics of resilience and hope during a centering meditation intervention.

Who can participate?
Adults enrolled at least part time in undergraduate or graduate school

What does the study involve?
The study involves daily access to the internet. It includes completing bi-daily brief assessments and 3 comprehensive mental wellness assessments online at pre-specified times. Treatment group will be asked to practice a 10-minute meditation every morning and night. Participants enrolled in study completed three measurement procedures: a) one-time demographics questionnaire, b) a bi-daily brief hope assessment, and c) an assessment battery at three points in time. Each assessment was available through a link to Qualtrics, which emailed them the assessments to participants at predesignated times. Once participants enrolled in the study, they completed a demographics survey followed by an initial assessment battery. They subsequently received a battery of assessments that measured resilience, stress, spiritual transcendence, and mindfulness. Qualtrics resent this assessment battery again at the mid-point and final point of the study. If participants did not respond to an assessment, Qualtrics sent an e-mail reminder to complete the survey with a new link. Lastly, participants also received a link to a brief assessment of hope every morning and evening for the entirety of the study, culminating in a total 56 administrations of four weeks. Over a four-week period, each participant received an email reminder to meditate in the morning at 6 am and in the evening at 6 pm. After meditating, they completed a brief online assessment of hope via Qualtrics. At the same windows of time, participants in the control group received the same brief assessments of hope without the reminder to meditate

What are the possible benefits and risks of participating?
There are no known risks associated with this study. Participants will be simply asked to respond to several survey items and participate in a brief exercise.

Where is the study run from?
William & Mary College (USA)

When is the study starting and how long is it expected to run for?
August 2020 to October 2020

Who is funding the study?
Investigator initiated and funded

Who is the main contact?
Stephanie Dorais, sdorais@email.wm.edu

Contact information

Dr Stephanie Dorais
Public

215 North Ave
Hillside
07205
United States of America

ORCiD logoORCID ID 0000-0002-0045-4278
Phone +1 (757) 932-0421
Email sdorais@kean.edu

Study information

Study designOnline single center interventional double-blind randomized controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Internet/virtual
Study typeTreatment
Participant information sheet Not available in web format, please use contact details to request a participant information sheet.
Scientific titleEffects of Centering Prayer Meditation compared to waitlist control on Resilience, Mindfulness, Stress, and Hope among college students
Study acronymCPMRMSH
Study hypothesis1. There will be a significant difference in resilience (as measured by the RSES) between a group of individuals who participate in a daily meditation and individuals from an intent-to-treat sample.
2. The fluctuations of hope (as measured by the SHS) will be non-stationary in the comparison group and they will stabilize and increase in trend in the treatment group.
3. Hope (as measured by the SHS) will serve as a significant explanatory variable and mediating variable in the trajectory of resilience over four weeks.
4. There will be a significant correlation between Centering Prayer and the constructs of mindfulness, spiritual transcendence, and stress.
Ethics approval(s)Approved 24/08/2020, William & Mary Institutional Review Board (200 Stadium Dr, Williamsburg, VA 23185, USA; +1 757 2213862; jastev@wm.edu), ref: EDIRC-2020-08-02-14426-sdorais
ConditionImprovement of resilience, stress, mindfulness, and hope among college students
InterventionParticipants are randomized through Qualtrics randomized generator into treatment or waitlist control group. The treatment group participated in a centering prayer meditation at home every morning and evening for 10 minutes for 4 weeks. They report their adherence through bi-daily assessments emailed them to them twice a day.
Intervention typeBehavioural
Primary outcome measureResilience is measured using the Response to Stressful Experience Scale at baseline, 2 weeks, and 4 weeks.
Secondary outcome measures1. Stress measured using Perceived Stress Scale at baseline, 2 weeks, and 4 weeks
2. Mindfulness measured using the Cognitive and Affective Mindfulness Scale- Revised at baseline, 2 weeks, and 4 weeks.
3. Spiritual Transcendence using the Spiritual Transcendence Scale at baseline, 2 weeks, and 4 weeks.
4. Hope using the State Hope Scale measured twice a day from baseline to Week 4.
Overall study start date24/08/2020
Overall study end date18/10/2020

Eligibility

Participant type(s)Healthy volunteer
Age groupAdult
Lower age limit18 Years
SexBoth
Target number of participants200
Total final enrolment190
Participant inclusion criteria1. Enrolled at least part time in college or graduate school
2. Over the age of 18 years
Participant exclusion criteria1. Individuals under the age of 18
2. Individuals not enrolled in an undergraduate or graduate program
Recruitment start date05/09/2020
Recruitment end date20/09/2020

Locations

Countries of recruitment

  • United States of America

Study participating centre

William and Mary
301 Monticello Ave
Williamsburg
23188
United States of America

Sponsor information

William & Mary
University/education

301 Monticello Ave
Williamsburg
23188
United States of America

Phone +1 757-221-3862
Email jastev@wm.edu
Website https://www.wm.edu
ROR logo "ROR" https://ror.org/03hsf0573

Funders

Funder type

Other

Investigator initiated and funded

No information available

Results and Publications

Intention to publish date30/09/2021
Individual participant data (IPD) Intention to shareYes
IPD sharing plan summaryAvailable on request
Publication and dissemination planPlanned publication in a high-impact peer-reviewed journal.
IPD sharing planThe datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request. sdorais@kean.edu. The data will include SAS outputs only of statistical analysis. There are no ethical or legal restrictions applicable.

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article 21/10/2021 12/04/2022 Yes No

Editorial Notes

12/04/2021: Publication reference added.
10/08/2021: Trial's existence confirmed by William & Mary Institutional Review Board