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The Effect of Art Therapy on Pain, Emesis, Anxiety and Quality of Life, Breast Cancer

NCT ID: NCT05666583

Last Updated: 2022-12-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-01

Study Completion Date

2022-10-07

Brief Summary

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The research sample consisted of 60 individuals, including the intervention group (n=30) and the control group (n=30), who received treatment at the Oncology Center of Sivas Cumhuriyet University Practice and Research Hospital. Personal Information Form, Pain Intensity Measurement-Visual Analog Scale, Rhodes nausea, vomiting and retching index, Beck Anxiety Inventory, FACT-G Quality of Life Scale were applied to the research data. Toxicity Rating Scale total score was recorded from the patient file. Within the scope of the research, a chemotherapy session for 10 weeks (5 sessions) with an interval of two weeks was made by the art expert of the art of marbling, accompanied by a ney concert. No intervention was made in the control group. Within the scope of the research, scale forms will be applied to both groups in the first interview, in the 3rd and 5th chemotherapy sessions of the patients. The data obtained from the study were uploaded to the SPSS (22.0) program and statistical evaluation was made.

Detailed Description

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Conditions

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Breast Cancer

Keywords

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Breast cancer, art therapy marbling art music therapy pain, emesis, anxiety quality of life

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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Intervention Group

Within the scope of the research, the art of marbling was made by the art expert, accompanied by a total of 5 sessions ney concerts for 10 weeks, with two-week intervals. The art application was made to last 20-30 minutes before the patients received chemotherapy. The scales were administered to the individuals in the intervention groups three times in total.

Group Type EXPERIMENTAL

Art therapy

Intervention Type OTHER

The intervention group is the group in which art therapy is applied. They receive chemotherapy.

Control Group

No treatment was applied to the control group. The scales were administered to the individuals in the control groups three times in total.

Group Type EXPERIMENTAL

Art therapy

Intervention Type OTHER

The intervention group is the group in which art therapy is applied. They receive chemotherapy.

Interventions

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Art therapy

The intervention group is the group in which art therapy is applied. They receive chemotherapy.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients who have received at least one course of chemotherapy, who have undergone breast surgery, who have not been given art therapy, who have no communication difficulties and no mental problems, who are 18 years of age or older, and who agreed to participate in the study.

Exclusion Criteria

* Those with cancer stage IV, visual, hearing and communication difficulties, those under the age of 18 and those who wanted to leave the study were not included in the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cumhuriyet University

OTHER

Sponsor Role lead

Responsible Party

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Esra Baser Akin

Research Asisstant (Researcher in the clinic)

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Esra BAŞER AKIN

Sivas, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Mollaog Lu MC, Mollaog Lu S, Akin EB, Mollaog Lu M, Yanmis S. The Effect of Art Therapy on Pain, Emesis, Anxiety, and Quality of Life in Operated Breast Cancer Patients: Randomized Control Trials. J Integr Complement Med. 2024 Apr;30(4):371-382. doi: 10.1089/jicm.2023.0062. Epub 2023 Oct 12.

Reference Type DERIVED
PMID: 37824754 (View on PubMed)

Other Identifiers

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2020-11/15

Identifier Type: -

Identifier Source: org_study_id