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The Effect of Stress Ball Application on Stress, Anxiety and Comfort During Chemotherapy in Women With Breast Cancer

The Effect of Stress Ball Application on Stress, Anxiety and Comfort During Chemotherapy in Women With Breast Cancer: A Randomized Controlled Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06460974
Enrollment
74
Registered
2024-06-14
Start date
2024-06-30
Completion date
2024-12-31
Last updated
2024-06-14

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

Conditions

Patients With Breast Cancer

Keywords

Anxiety, Comfort, Breast Cancer, Stress, Stress Ball

Brief summary

This research was conducted as a randomized controlled study to determine the effect of stress ball application on stress, anxiety and comfort in women with breast cancer receiving chemotherapy.

Detailed description

The research was conducted as a randomized controlled study. A total of 74 patients were randomly assigned to the stress ball group (n=37) and the control group (n=37).

Interventions

OTHERstress ball

A stress ball was applied to the patients in the during chemotherapy treatment.

Sponsors

Mersin University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* who is literate in Turkish, * who was diagnosed with stage 1, 2 and 3 breast cancer * who had the second cure or above chemotherapy receiving treatment * over 18 years of age * female * platelet level \>50,000 mm3 * not having any physical problems squeezing a stress ball

Exclusion criteria

* those who did not agree to participate in the study * those who received chemotherapy for the first time, * those who had any physical disability to squeeze a stress ball * Any receiving intravenous treatment from both arms, * having had a unilateral or bilateral mastectomy and having a problem squeezing a stress ball, * having any psychiatric disease,

Design outcomes

Primary

MeasureTime frameDescription
Distress Thermometer6 monthsDistress level is determined by a visual analog scale ranging from 0-10. Patients express the psychological distress they feel with the numbers on the thermometer; 0 points means that the patient does not experience any distress, and 10 points means that the patient experiences the highest level of distress
State-Trait Anxiety Inventory6 monthsIt evaluates the state of anxiety felt by the individual due to the stressful situation he is in. The first 20 items, consisting of short statements, measure the individual's state anxiety level.
General Comfort Scale6 monthsThe scale contains a total of 48 items in a four-point Likert type and consists of four sub-dimensions (physical, psycho-spiritual, environmental, and socio-cultural sub-dimensions).

Countries

Turkey (Türkiye)

Contacts

Primary ContactBirgül VURAL DOĞRU
bvuraldogru@gmail.com03243610001

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026