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Effects of providing positive informations to deal with cancer on psychological wellbeing and physiological stress responses among women with reproductive cancer.

Phase 1
Conditions
The participants of this study are women with reproductive cancer who are admitted at Oncology ward, Saraburi Hospital The decision whether to participate in this study depends on their willingness The intervention in this study is no injury to any participant because intervention of this study is positive information The instruments in this study used for measuring in this study are a questionnaire. During data collection process, the researcher will observe the participants&#039
facial expressions, abnormal sign and symptoms, and behavioral changes or if the participant feel discomfort immediately or sad, unhappy, etc. they can report to research and can stop and take a rest. However, if distress symptoms of the participants do not improve, the research will consult ward nurse, specialist consultant, or doctors to solve the problems
Positive information, Hope, Happiness, Anxiety, Physiological stress responses, and women with reproductive cancer
Registration Number
TCTR20230828001
Lead Sponsor
Graduate school Financial Support for Thesis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending (Not yet recruiting)
Sex
Female
Target Recruitment
108
Inclusion Criteria

The participants of this study will be selected according to the inclusion criteria The inclusion criteria consist of 1 women with reproductive cancer between the ages of 30 to 80 years 2 Thai women who are Buddhist 3 diagnosed with cervical cancer corpus uteri cancer or ovarian cancer in the stages 1 to 3 and 4 can see (not blind) and hear not deaf
During the time the participants are treated if they feel any pain, tiredness nausea unhappiness or experience severe vomiting after receiving the treatment the researcher will wait for the patient's condition to improve and reconsider their participation in the study In addition the participants must not receive drugs that affect physiological stress responses such as steroids prednisolone betamethasone etc However if the half-life of a steroid drug is approximately 1 to 3 and half hours then these participants can still participate in this study

Exclusion Criteria

The women with reproductive cancer who cannot attend all of the class of intervention or who feel upset during study will be excluded and give emotional support

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hope at 5 minutes after end of intervention 100 mm Hope VAS score,Happiness at 5 minutes after end of intervention 100 mm Happiness VAS score,Anxiety at 5 minutes after end of intervention State Anxiety Inventory in Thai version score,Physiological stress responses at 5 minutes after end of intervention Sphygmomanometer score
Secondary Outcome Measures
NameTimeMethod
Blood pressure at 2 minutes after end of intervention Sphygmomanometer
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