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Not yet recruiting NCT07672340

Care Burden And Qualıty of Lıfe

No phase Interventional Caregiver Burden Quality of Life Public Health

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Health Promotion Behavior Education.
Who it may be relevant to
Registry conditions: Caregiver Burden, Quality of Life, Public Health. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect Of Multıdımensıonal Traınıng Applıed to Caregıvers of Home Health Servıce Recıpıents Aged 65 And Over on Care Burden And Qualıty of Lıfe

Overview

This randomized controlled trial will be conducted to examine the effect of a multidimensional training program, to be implemented by a public health nurse, on the care burden and quality of life of primary caregivers of patients aged 65 and older.

Interventions

  • Behavioral Health Promotion Behavior Education
    Personal hygiene, hand hygiene, Musculoskeletal system, body mechanics, relaxation exercises, the importance of physical activity, Proper and healthy nutrition, foods to increase and decrease consumption of, food safety and hygiene, Sleep health, sleep hygiene, the importance of sleep in human life, sleep quality, sleep duration, and factors affecting sleep, Early detection methods, adult immunization, rational use of medications, Safe environment and home accidents.

Primary outcome measures

  • Before intervention caregiving burden [Time frame: Before intervention]
  • After intervention caregiving burden [Time frame: 1 week after intervention]
Secondary outcome measures (2)
  • Before intervention [Time frame: Before intervention]
  • After intervention [Time frame: 1 week after intervention]

Eligibility criteria

Inclusion criteria

Be willing to participate in the study

  • Be literate
  • Have registered with a home health care unit
  • Have been responsible for the care of a relative aged 65 or older for at least one month
  • Score at least 21 on the Zarit Caregiver Burden Scale

Exclusion criteria

  • • Having severe reading comprehension difficulties
  • Having severe hearing difficulties
  • Having been diagnosed with a psychiatric disorder (schizophrenia, bipolar disorder, or anxiety disorder)
  • Failing to complete the data collection instruments used in the study
  • Failing to attend at least two training sessions

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07672340 · 10.01.2024-1389-1409 · HF-24005

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗