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The Effect of MIND-BE Program on Mental Health Parameters (Mindfulness Based Empowerment)

NCT04987905 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2022-06-03

No results posted yet for this study

Summary

This study will be carried out in a pre-test-post-test, randomized controlled (parallel), experimental order in order to examine the effect of the MIND-BE program applied to intensive care nurses on mental health parameters. The hypothesis of this study is that MIND-BE program increases resilience, posttraumatic growth, mindfulness, self-compassion levels, and reduces mental symptoms.

Conditions

  • Resilience
  • Posttraumatic Growth
  • Mindfulness
  • Self-compassion
  • Mental Health

Interventions

OTHER

Mindfulness

In the study, for 60 minutes once a week for 8 weeks MIND-BE program will be applied to nurses. The program includes formal and informal practices of mindfulness ("Getting started, Introduction to MIND-BE, Noticing the autopilot, Power of attention, Simple awareness, Eating awareness, Body awareness, Breath awareness, Sitting awareness, Stress and reactions, Vision awareness, Challenging emotions and situations in business life, Awareness in business life, Awareness and communication, Awareness and compassion, Developing your own practice).

Sponsors & Collaborators

  • Mersin University

    collaborator OTHER

  • Hilal Altundal

    lead OTHER

Principal Investigators

  • Mualla Yılmaz, Professor · Mersin University, Faculty of Nursing, Ciftlikkoy Campus, 33343, Yenisehir, Mersin

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-04-13
Primary Completion
2021-09-24
Completion
2022-03-31

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04987905 on ClinicalTrials.gov