New nursing method eases caregiver burnout in brain injury cases
NCT ID NCT07507357
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a special nursing approach, called the Tidal Model, to help caregivers of people with traumatic brain injury. 18 caregivers took part and the program aimed to reduce their anxiety, depression, and burnout. The approach focused on understanding each caregiver's personal experiences and providing support.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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18 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Mar 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Providing care for an individual diagnosed with Traumatic Brain Injury (TBI). Being between the ages of 18 and 65. Having provided care for the patient for at least 3 months. Volunteering and providing informed consent to participate in the study. Being proficient in speaking and understanding Turkish. Having no cognitive or physical impairments that would hinder effective communication. Exclusion Criteria: Being under the age of 18 or over the age of 65. Having provided care for less than 3 months. Being illiterate or unable to read and write. Providing care for an individual with a diagnosis other than Traumatic Brain Injury (TBI). Unwillingness to participate in the study or refusal to provide informed consent. Failure to fully complete the required study forms and measurement scales.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Gaziler Physical Medicine and Rehabilitation Training and Research Hospital
Ankara, ÇANKAYA, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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