Skip to main content
Clinical Trials/NCT01590524
NCT01590524
Completed
N/A

Randomized Control Trial for the Effect of Guided Imagery and Progressive Muscle Relaxation in Reducing Anxiety for Parents of Hospitalized Children With Cancer

Cyprus University of Technology1 site in 1 country52 target enrollmentApril 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Anxiety
Sponsor
Cyprus University of Technology
Enrollment
52
Locations
1
Primary Endpoint
Changes in the number of Participants with anxiety
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to determine whether Guided Imagery and Progressive Muscle relaxation are effective as stress reducing techniques in parents of hospitalized children with cancer.

Detailed Description

Having a children with cancer can be a source of stress for parents during hospitalization. The stress experienced by the parents can negatively influence their functionality, daily activities, psychological state and also their physical condition. The studies in the literature have mainly focused on the child rather than the parent, and studies specifically for guided imagery are scarce. Since the parents are often neglected by the healthcare professionals during the stress evoking period of hospitalization, this study will test the effectiveness of complementary methods in improving the psychological state of the parents.

Registry
clinicaltrials.gov
Start Date
April 2012
End Date
October 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Andreas Charalambous

Lecturer-Researcher

Cyprus University of Technology

Eligibility Criteria

Inclusion Criteria

  • willingness to participate
  • having a child with childhood cancer been hospitalized for 4 weeks
  • have a child (0-18) of age with childhood cancer
  • able to speak and write Greek fluently
  • no previous experience with CAM techniques

Exclusion Criteria

  • receiving drug therapy for stress
  • using another CAM technique during the study
  • parents of children receiving palliative care

Outcomes

Primary Outcomes

Changes in the number of Participants with anxiety

Time Frame: 1 week, 2 week, 3 week , 4 week

Participants response to the complementary and alternative intervention will be measured through their scores on the Hamilton Anxiety Scale

Secondary Outcomes

  • Changes in the number of Participants with mood changes(1 week, 2 week, 3 week , 4 week)
  • stress level with Biodots(1 week, 2 week, 3 week, 4 week)

Study Sites (1)

Loading locations...

Similar Trials