| Registry | NCT06977867, acronym Stress Ball |
|---|---|
| Status | Enrolling by invitation |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: none, supportive care |
| Enrollment | 36 (Estimated) |
| Sponsor | Bitlis Eren University (Other) |
| Conditions | Hemodialysis Patients |
| Interventions | Stress Ball, standard care (Device, other) |
| Dates | start 2025-05-01, primary completion 2025-09-01 (estimated), completion 2025-09-30 (estimated), first posted 2025-05-18, last updated 2025-05-21 |
| Locations | 1 site in Turkey (Türkiye) |
Related Papers Related Patents Related Grants Related Experts
All trials for Hemodialysis Patients All trials of Stress Ball All trials of standard care
Chronic kidney disease represents a significant public health issue both in Türkiye and worldwide, with the majority of patients undergoing hemodialysis treatment. Individuals receiving hemodialysis often experience not only physical discomfort but also psychological distress, including heightened anxiety and reduced comfort. The aim of this study is to evaluate the effects of stress ball use on comfort, anxiety, and patient satisfaction among hemodialysis patients. The stress ball is a simple and cost-effective non-pharmacological intervention that aids individuals in managing stress by redirecting their attention. Notably, this study is unique in simultaneously investigating comfort, anxiety, and satisfaction parameters within this patient population.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Stress Ball | Experimental | Device: Stress Ball | All hemodialysis patients who meet the inclusion criteria will be asked to squeeze a stress ball during their dialysis sessions (3 times a week for 1 month, totaling 12 sessions). Anxiety, comfort, and patient satisfaction levels will be assessed using three measurements: a pre-test before the intervention, a mid-test at the end of the 6th session (2nd week), and a post-test after the 12th session. Patients will be instructed to use the stress ball throughout their dialysis session. They will be asked to squeeze the ball for at least 10-15 minutes during each session. |
| Control | Other | Other: standard care | The hemodialysis patients in the control group will not use the stress ball and will receive standard care throughout the study period. Similar to the intervention group, levels of anxiety, comfort, and patient satisfaction will be assessed at three time points: prior to the intervention (pre-test), at the end of the second week (after the 6th session), and at the end of the fourth week (post-test, after the 12th session). |
Sex: All, ages: 18 Years to 98 Years, accepts healthy volunteers
Inclusion Criteria: * Being 18 years of age or older * Being literate * Having no visual or hearing impairments * Being able to communicate verbally * Having no physical disability that would prevent the use of a stress ball * Not having a diagnosed anxiety disorder and not using medication for it * Willingness to participate in the study Exclusion Criteria: * Currently using sedative medications * Having a diagnosed psychiatric disorder * Having any physical limitation that prevents squeezing a stress ball
| Facility | City | Country | Status |
|---|---|---|---|
| Bitlis State Hospital | Bitlis, Tatvan | Turkey (Türkiye) |