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The Impact of a Web-based Empowerment Program on Intolerance of Uncertainty and Maintenance Burden.

The Effect of a Web-Based Empowerment Program Based on the Theory of Illness Applied to Caregivers of Prostate Cancer Patients on Intolerance of Uncertainty and Caregiver Burden: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07668427
Enrollment
62
Registered
2026-06-25
Start date
2026-07-01
Completion date
2027-05-17
Last updated
2026-06-25

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

Conditions

Caregiving Burden, Intolerance of Uncertainty

Keywords

Intolerance of uncertainty, caregiving burden

Brief summary

The aim of this study is to examine the relationship between uncertainty intolerance and caregiver burden in a web-based empowerment program based on uncertainty theory in disease, applied to caregivers of prostate cancer patients.

Detailed description

This study was designed as a pre-test-post-test parallel-group, randomized controlled experimental design. The research will be conducted at the Radiation Oncology Clinic of Necmettin Erbakan University Faculty of Medicine Hospital, Republic of Turkey. Caregivers of prostate cancer patients will be randomly divided into two groups: experimental group (31) and control group (31). For the experimental group: A web-based reinforcement program based on uncertainty theory will be applied. For the control group: No application will be made to the caregivers. The primary outcome of this study is to determine the intolerance to uncertainty scores of caregivers of prostate cancer patients. The secondary outcome is to determine the caregiving burden of caregivers.

Interventions

OTHERWeb-Based Empowerment Program Based on Uncertainty Theory

Web-Based Empowerment Program Based on Uncertainty Theory

Sponsors

Necmettin Erbakan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Parallel Assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Over 18 years of age, * Able to speak Turkish, * Literate, * No hearing or vision problems, * No neurological and/or psychiatric disorders, * Physical and cognitive health levels suitable for answering the forms used in the study, * Having a patient diagnosed with prostate cancer, * Being the primary caregiver responsible for meeting the patient's care needs (home care, supervision, hospital check-ups, etc.) within the family, * Having a patient scheduled for hormone therapy and radiotherapy, * Not having undergone prostatectomy, * Having an electronic device such as a smartphone or computer with internet access, either themselves or a family member, * Caregivers of prostate cancer who volunteer to participate in the study will be included.

Exclusion criteria

* Caregivers whose patients are receiving chemotherapy will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Intolerance of Uncertainty Scalefirst week and fifteenth weekThe highest possible score on the scale is 60, and the lowest is 12. Higher scores indicate a high level of intolerance for uncertainty. Higher scores indicate greater intolerance for uncertainty.

Secondary

MeasureTime frameDescription
Zarit Caregiver Burden Scalefirst week and fifteenth weekThe scale can be scored from a minimum of 0 to a maximum of 88 points. A high score on the scale indicates a high caregiver burden.

Contacts

CONTACTKübra Nur KÖSE ALABAY
kubranurkosee@hotmail.com+905544319384

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 26, 2026