MedPath

Feasibility Study on the Effect of Complementary Methods as Supportive Interventions for Parents of Children With Cancer

Not Applicable
Completed
Conditions
Anxiety
Stress
Mood
Coping
Interventions
Behavioral: Guided Imagery and Progressive Muscle Relaxation
Registration Number
NCT01590524
Lead Sponsor
Cyprus University of Technology
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
52
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
CAM groupGuided Imagery and Progressive Muscle RelaxationSubjects receiving the interventions and standard psychological care
Primary Outcome Measures
NameTimeMethod
Changes in the number of Participants with anxiety1 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 Outcome Measures
NameTimeMethod
Changes in the number of Participants with mood changes1 week, 2 week, 3 week , 4 week

Participants response to the complementary and alternative interventions will be measured through their scores on the POMS scale

stress level with Biodots1 week, 2 week, 3 week, 4 week

Trial Locations

Locations (1)

Archbishob Makarios Hospital

🇨🇾

Nicosia, Cyprus

© Copyright 2025. All Rights Reserved by MedPath