The Effect of the Hand Massage A Women Undergoing Brachytherapy
NCT ID: NCT05937607
Last Updated: 2023-07-10
Study Results
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Basic Information
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UNKNOWN
NA
36 participants
INTERVENTIONAL
2023-06-14
2023-08-15
Brief Summary
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Methods This parallel-group randomized controlled study evaluated the effect of the hand massage practiced using baby oil, with lavender oil, on reducing operational pain and situational anxiety in women with brachytherapy. The study was completed with 36 patients. The treatment group included 18 patients, and the control group had 18. The data were collected through patient information form, visual analog scale, and state anxiety inventory. Before the brachytherapy, three sessions of hand massages, each lasting 10 minutes (5 minutes for each hand), were performed using baby oil with lavender. Data collection forms were repeated after each session. The control group received routine treatment. p\<0.05 was accepted as significant.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Hand massage
hand massage was applied to the patients to receive intracavitary brachytherapy using lavender baby oil for three sessions of 10 minutes each, starting 5 minutes before the procedure.
Hand massage
It is reported in the literature that the application should last 5-10 minutes on average to reduce acute pain, state anxiety, and provide physiological positive changes and relaxation in individuals during the procedure
Control Group
The control group did not receive any intervention during the study period
No interventions assigned to this group
Interventions
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Hand massage
It is reported in the literature that the application should last 5-10 minutes on average to reduce acute pain, state anxiety, and provide physiological positive changes and relaxation in individuals during the procedure
Eligibility Criteria
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Inclusion Criteria
* to be at the age of 18 and above
* to be diagnosed with gynecologic cancer and receive BT three days a week regularly
* to be aware that she has a gynecologic cancer disease and to be a volunteer to participate in the study
Exclusion Criteria
* received complementary and integrated treatment
* had edema or lesion on hand, had a psychiatric disease
* had communication problems
* did not want to have a massage
* were under general anesthesia during the intervention
18 Years
FEMALE
Yes
Sponsors
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TC Erciyes University
OTHER
Responsible Party
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Dilek Efe Arslan
Principal Investigator
Principal Investigators
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DİLEK EFE ARSLAN, PhD
Role: STUDY_DIRECTOR
ERCİYES UNİVERSİTY
Locations
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Dilek Efe Arslan
Kayseri, Talas, Turkey (Türkiye)
Countries
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Other Identifiers
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815/795
Identifier Type: -
Identifier Source: org_study_id
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