Skip to content

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

Effects of providing positive information to deal with cancer on hope, happiness, anxiety, and physiological stress responses among women with reproductive cancer: A randomized controlled trial.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230828001
Enrollment
108
Registered
2023-08-28
Start date
2023-08-28
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

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

Interventions

In experimental group will receive individual providing information from the researcher in the afternoon on the following topics: A video record of 3 women with survival from cancer for 50 minutes an
Experimental Other,Experimental Other
Intervention name is provide positive informations ,Intervention is usual care from ward nurse

Sponsors

Graduate school Financial Support for Thesis
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: The participants of this study will be selected according to the inclusion criteria The inclusion criteria consist of as follow: 1. The participants in this study were women with reproductive cancer between the ages of 15 to 80 years. 2. The participants in this study were Thai women who are Buddhist. 3. The diagnoses of the participants in this study were cervical cancer corpus uteri cancer or ovarian cancer in stages 1 to 3. 4. The participant in this study 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

Exclusion criteria: The women with reproductive cancer who as follow: 1. They cannot attend all of the class of intervention. 2. If who feel upset during study will be excluded and give emotional support.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Blood pressure at 5 minutes after end of intervention Sphygmomanometer

Countries

Thailand

Contacts

Public ContactNatchira Winitchai

Suranaree University of Technology

natchira@sut.ac.th6644223991

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026