Comparison of Social Media-Based and Online Training in Grief Counseling Education
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorIstinye University
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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.
Disqualifiers
Previous training in perinatal grief counseling.
Failure to participate regularly in the educational intervention.
Failure to complete the study assessments.
Trial design
Design model
Parallel
Treatments tested in this trial
Social Media-Based Perinatal Grief Counseling Education
BehavioralA six-week structured perinatal grief counseling education program delivered through Instagram using asynchronous posts, stories, reels, videos, quizzes, and interactive activities.
Online Perinatal Grief Counseling Education
BehavioralA six-week structured perinatal grief counseling education program delivered through synchronous Zoom sessions, including presentations, case discussions, interactive activities, and role-play exercises.
Treatment groups
72 Participants
are divided into 2 treatment groupsGroup A: Social Media-Based Education GroupExperimental treatment 1 intervention
Group B: Online Education GroupExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Perinatal Bereavement Care Competency
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.
Time frame
Baseline, immediately after completion of the 6-week intervention, and 4 weeks after the intervention.2
Perinatal Bereavement Care Confidence
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.
Time frame
Baseline, immediately after completion of the 6-week intervention, and 4 weeks after the intervention.Secondary outcomes
1
Participant Evaluation of the Educational Program
Participants' evaluation of the educational program using a researcher-developed Education Evaluation Form.
Time frame
Immediately after completion of the 6-week intervention.Sponsors and contacts
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Source ClinicalTrials.gov
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