Comparison of Social Media-Based and Online Training in Grief Counseling Education

July 23, 2026 updated by: Ayşe İrem Gökçek, Istinye University

Comparison of Social Media-Based and Online Training in Grief Counseling Education: A Randomized Controlled Head-to-Head Study

This randomized trial aims to compare the effectiveness of two digital educational approaches for perinatal grief counseling training among midwives and nurses working in perinatal care settings in Türkiye: a social media-based education program delivered through Instagram and an online education program delivered through Zoom. Both groups will receive the same six-module perinatal grief counseling education content, but through different delivery methods.

Participants will be randomly assigned to one of the two study groups. Outcomes will be assessed before the intervention, immediately after completion of the 6-week training program, and 4 weeks after the intervention. The study will evaluate changes in participants' competency and confidence in providing perinatal grief care and compare the sustainability of learning outcomes between the two digital education models.

Study Overview

Detailed Description

Perinatal loss can have profound psychological effects on affected families. Midwives and nurses play an important role in providing emotional support and grief care following perinatal loss. However, healthcare professionals may have limited training and confidence in providing perinatal grief counseling. Structured education may improve their competency and confidence in delivering bereavement care.

This study will compare a competency-based perinatal grief counseling education program delivered through two digital models: social media-based learning using Instagram and synchronous online learning using Zoom. The educational content was developed from a previously validated competency framework established through a Delphi consensus study. Both groups will receive the same six-module educational content and learning objectives; only the mode of delivery will differ.

The study is designed as a two-arm randomized trial. Participants will complete assessments before the intervention, immediately after the training, and four weeks after completion of the intervention. The study will examine whether the digital delivery method affects competency and confidence in providing perinatal grief care and whether the learning outcomes are maintained over time.

Study Type

Interventional

Enrollment (Estimated)

72

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Midwives or nurses currently working in perinatal care settings in Türkiye.
  • Aged 18 years or older.
  • Own a smartphone and have regular internet access.
  • Able to actively use Instagram and Zoom.
  • Provide informed consent to participate in the study.

Exclusion Criteria:

  • Previous training in perinatal grief counseling.
  • Failure to participate regularly in the educational intervention.
  • Failure to complete the study assessments.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Social Media-Based Education Group
Participants in this group will receive a six-week perinatal grief counseling education program through a private Instagram account. Educational content will be delivered using posts, stories, reels, videos, quizzes, and interactive activities.
A six-week structured perinatal grief counseling education program delivered through Instagram using asynchronous posts, stories, reels, videos, quizzes, and interactive activities.
Experimental: Online Education Group
Participants in this group will receive the same six-module perinatal grief counseling education program through synchronous Zoom sessions over six weeks. Sessions will include presentations, case discussions, interactive activities, and role-play exercises.
A six-week structured perinatal grief counseling education program delivered through synchronous Zoom sessions, including presentations, case discussions, interactive activities, and role-play exercises.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perinatal Bereavement Care Competency
Time Frame: Baseline, immediately after completion of the 6-week intervention, and 4 weeks after the intervention.
This scale was developed by Shen et al. in 2022 to measure the grief care competence of midwives providing care to women experiencing perinatal death. Gökçek and Keser Özcan established its Turkish validity and reliability. The scale consists of 23 items and has six sub-dimensions: Maintaining Faith, Knowing, Being Together, Maintaining Esteem, Empowerment, and Self-Regulation. Each item is answered using a five-point Likert scale (Strongly Disagree=1, Disagree=2, Undecided=3, Agree=4, Strongly Agree=5), resulting in a minimum score of 23 and a maximum score of 115. Higher scores indicate greater competence in perinatal grief counselling. The Cronbach's alpha coefficient of the scale ranged from 0.69 to 0.87 for the sub-dimensions and was 0.92 for the entire scale.
Baseline, immediately after completion of the 6-week intervention, and 4 weeks after the intervention.
Perinatal Bereavement Care Confidence
Time Frame: Baseline, immediately after completion of the 6-week intervention, and 4 weeks after the intervention.
This scale, developed by Kalu et al. in 2019, measures midwives' and nurses' perceived competence in providing care to families experiencing perinatal loss. Dursun and Akkuş conducted the Turkish adaptation and reliability study of the scale. The scale consists of 35 items across four sub-dimensions: knowledge of grief support, grief support skills, self-awareness, and organizational support. Items are rated on a 5-point Likert scale (1=strongly disagree, 5=strongly agree). Some statements are reverse scored (e.g., items 7, 11, and 33). Each sub-dimension is evaluated independently, and the total score is not calculated. In the original scale development study, the Cronbach's alpha coefficients for the sub-dimensions ranged from 0.70 to 0.87.
Baseline, immediately after completion of the 6-week intervention, and 4 weeks after the intervention.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participant Evaluation of the Educational Program
Time Frame: Immediately after completion of the 6-week intervention.
Participants' evaluation of the educational program using a researcher-developed Education Evaluation Form.
Immediately after completion of the 6-week intervention.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

July 27, 2026

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

December 30, 2026

Study Registration Dates

First Submitted

July 20, 2026

First Submitted That Met QC Criteria

July 20, 2026

First Posted (Actual)

July 23, 2026

Study Record Updates

Last Update Posted (Actual)

July 24, 2026

Last Update Submitted That Met QC Criteria

July 23, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • EBE_ISU_1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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