- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07072078
- Original Trial
The Role of Nurses in Video-Based Communication to Reduce Loneliness in Intensive Care Unit Patients (VBC-ICU)
The Effect of Video-Based Communication on Reducing Loneliness in Intensive Care Unit Patients: A Quasi-Experimental Study
This study aims to evaluate the effectiveness of video-based communication in reducing loneliness among intensive care unit (ICU) patients at Dr. Hasan Sadikin General Hospital in Bandung, Indonesia. ICU patients often experience psychological distress, particularly loneliness, due to restricted family visits and physical isolation.
A quasi-experimental design with a pre-test and post-test control group is used, involving 36 participants who are randomly assigned to either the intervention or control group. The intervention group receives structured video-based communication with family members for three consecutive days, with each session lasting between 5 to 20 minutes. Nurses facilitate the intervention by ensuring patient safety, providing emotional support, and assisting with the communication process. The control group receives standard ICU care without the communication intervention.
Loneliness levels are assessed using the De Jong Gierveld Loneliness Scale (DJGLS) before and after the intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study investigates the effectiveness of video-based communication in reducing loneliness among patients in the Intensive Care Unit (ICU). Loneliness is a common psychosocial issue in ICU patients, caused by physical isolation, limited visitation policies, and minimal social interaction. It is associated with increased stress, potential suppression of immune response, and extended hospitalization. The intervention provides a practical approach by enabling virtual interaction with family members, allowing emotional connection despite physical distance.
The study uses a quasi-experimental design with a pre-test and post-test control group. A total of 36 patients are recruited from Dr. Hasan Sadikin General Hospital in Bandung and randomly assigned to either an intervention or control group. The intervention group receives structured video-based communication using WhatsApp for three consecutive days, with each session lasting between 5 and 20 minutes. The control group receives standard ICU care without the additional communication support. The De Jong Gierveld Loneliness Scale (DJGLS) is used to assess emotional and social loneliness levels before and after the intervention.
Nurses act as primary facilitators in the intervention. Their responsibilities include ensuring clinical stability, setting up the communication devices, emotionally supporting patients during the sessions, monitoring patient responses, documenting the process, and coordinating communication with family members.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Jawa Barat
-
Bandung, Jawa Barat, Indonesia, 40161
- dr. Hasan Sadikin General Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients admitted to the intensive care unit (ICU)
- Patients aged over 18 years with a minimum of 72 hours of care in the ICU
- Patients who are able to understand and communicate in the Indonesian language
Exclusion Criteria:
- Patients with medical conditions such as decreased consciousness, total blindness, or severe neurological disorders
- Patients with a history of psychiatric disorders
Drop Out:
- Patients who are discharged from the ICU of Dr. Hasan Sadikin General Hospital during the study period will be considered drop-outs
- Patients whose health deteriorates to the extent that they are unable to continue participation in the study
- Patients who die during the study period
- Patients who are transferred from the ICU to general inpatient wards
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group - Video-based Communication
Participants in this group received structured video-based communication with their family members using WhatsApp.
Each session lasted 5-20 minutes and was conducted once daily for three consecutive days.
The communication was facilitated by a nurse and included positive messages, emotional support, and discussion of future plans.
The aim was to reduce emotional and social loneliness in ICU patients.
|
Participants received structured video-based communication sessions with their family members using the WhatsApp platform.
The intervention was delivered once daily for three consecutive days, with each session lasting between 5 and 20 minutes.
Communication was guided to include emotional support, positive conversations, and future-oriented discussion.
The sessions were facilitated by nurses who ensured clinical stability, technical setup, and emotional readiness of the patient.
This intervention aimed to reduce emotional and social loneliness among ICU patients and was integrated into standard intensive care routines without disrupting medical care.
|
|
No Intervention: Control Group - Standard ICU Care
Participants in this group received standard ICU care without any video-based communication intervention.
They continued with routine treatment and monitoring in the ICU setting for the duration of the study period.
This group was used as a comparison to assess the impact of video-based communication on loneliness levels.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Loneliness Score (De Jong Gierveld Loneliness Scale)
Time Frame: Baseline (Day 1) to Post-Intervention (Day 3)
|
This outcome measures the change in loneliness among ICU patients before and after the intervention, using the De Jong Gierveld Loneliness Scale (DJGLS).
The scale assesses both emotional and social loneliness with 11 items, validated in Indonesian.
Higher scores indicate greater loneliness.
The score is recorded at baseline (pre-intervention) and after 3 days of intervention (post-test).
The difference in mean scores is used to assess effectiveness.
|
Baseline (Day 1) to Post-Intervention (Day 3)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Cecep Eli Kosasih, S.Kp., MNS., Ph.D, Universitas Padjadjaran
- Study Director: Ristina Mirwanti, S.Kep., Ners., M.Kep., Universitas Padjadjaran
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NURS-202506.01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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