Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07383935

Stress Ball Use During Chemotherapy in Gastrointestinal Cancer Patients

Led by Artvin Coruh University · Updated on 2026-02-11

60

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will investigate whether using a stress ball during chemotherapy can reduce anxiety, fear, and changes in vital signs in patients with gastrointestinal system cancers. Patients receiving chemotherapy for gastrointestinal cancers often experience anxiety and fear, which may affect their heart rate, blood pressure, and breathing. A stress ball is a simple, low-cost, and safe method that may help patients relax during treatment. In this randomized controlled study, 60 patients receiving chemotherapy will be assigned to either a stress ball group or a routine care group. Patients in the stress ball group will squeeze a stress ball for 15 minutes during their chemotherapy session. Anxiety, fear levels, and vital signs will be measured before and after chemotherapy in both groups. The results of this study may help determine whether stress ball use is an effective non-drug method to improve emotional well-being and physiological stability in patients undergoing chemotherapy.

CONDITIONS

Official Title

Stress Ball Use During Chemotherapy in Gastrointestinal Cancer Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be 18 years or older
  • Have a diagnosis of gastrointestinal system cancer and be receiving chemotherapy
  • Have no communication problems
  • Have no physical disability that would prevent squeezing a stress ball
  • Be willing to participate in the study
Not Eligible

You will not qualify if you...

  • None specified

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Artvin State Hospital

Artvin, Turkey (Türkiye)

Actively Recruiting

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Research Team

E

Efe Hasdemir Efe Hasdemir, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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