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The effect of Guided Imagery on Nausea and Vomiting and Quality of Life in Cancer Chemotherapy

Not Applicable
Recruiting
Conditions
Condition 1: Chemotherapy-induced Nausea and Vomiting in Cancer. Condition 2: Quality of Life in Cancer patients undergoing Chemotherapy.
Neoplasms of unspecified behavior
C00-D49
Registration Number
IRCT20200710048073N1
Lead Sponsor
Bagheiat-allah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

Age above 18 years and under 65 years
Minimum Education Level
Willingness to participate in research
Nausea and Vomiting experience during the Chemotherapy
At least one session of Chemotherapy is performed and at least one course of Chemotherapy has left after enrollment

Exclusion Criteria

Use of Nausea and Vomiting Medications other than routine and use of Complementary Medications such as Ginger
Gastrointestinal Cancer
Performing Radiotherapy simultaneously with Chemotherapy
Hearing disorders
History of Gastrointestinal Surgery
Gastrointestinal Cancer
History of mental disorder
The participant is a member of the Healthcare team
Have taken psychological skills training courses such as relaxation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea and Vomiting. Timepoint: Pre-intervention? post-intervention and two months after the intervention. Method of measurement: Nausea and Vomiting Questionnaire (The Multinational Association of Supportive Care in Cancer.;Quality of Life. Timepoint: Pre-intervention and two months after the intervention. Method of measurement: Quality of Life Questionnaire - ( European Organization for Research and Treatment of Cancer).
Secondary Outcome Measures
NameTimeMethod
ausea and Vomiting. Timepoint: Pre-intervention and after Chemotherapy and two months after the intervention. Method of measurement: Questionnaire Antiemesis Tool- The Multinational Association of Supportive Care in Cancer -.;Quality of Life. Timepoint: Pre-intervention and two months after the intervention. Method of measurement: Quality of Life Questionnaire - ( European Organization for Research and Treatment of Cancer).
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