Description Module

Description Module

The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.

Description Module path is as follows:

Study -> Protocol Section -> Description Module

Description Module


Ignite Creation Date: 2025-12-24 @ 4:41 PM
Ignite Modification Date: 2025-12-24 @ 4:41 PM
NCT ID: NCT06215066
Brief Summary: A randomized controlled trial with two parallel groups was conducted, to determine the effect of virtual reality (VR) and modified progressive muscle relaxation (MPMR) distraction techniques on anxiety, attention and getting distracted from the external environment among cardiac care unit patients. The study is based on the following hypotheses: H1: Patients who receive VR intervention have lower Hamilton Anxiety Rating (HAM-A) scores than those who receive MPMR intervention. H2: Patients who receive VR intervention exhibit improvement in their physiological parameters than those who receive MPMR intervention. H3: Patients who receive VR intervention have higher Attention/Distraction scores than those who receive MPMR intervention.
Detailed Description: This randomized controlled trial with two parallel groups was conducted in the cardiac care unit of Smouha Hospital, affiliated with Alexandria University, Egypt. A total of 158 patients were recruited using a simple random sampling method and assigned to one of two groups to determine the effects of virtual reality (VR) and modified progressive muscle relaxation (MPMR) distraction techniques on anxiety, attention, and distraction from the external environment among cardiac care unit patients. Four assessment tools were used: 1. Sociodemographic and Clinical Assessment. 2. Physiological Parameter Assessment. 3. Hamilton Anxiety Rating Scale (HAM-A). 4. Attention/Distraction Scale.
Study: NCT06215066
Study Brief:
Protocol Section: NCT06215066