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Care Burden And Qualıty of Lıfe (Care Burden)

24. juni 2026 opdateret af: Dilek Hassoy, Aydin Adnan Menderes University

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

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.

Studieoversigt

Status

Ikke rekrutterer endnu

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

78

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Støttende pleje
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Kontrolgruppe
Kontrolgruppen fortsatte med at modtage den rutinemæssige pleje
Eksperimentel: Structured education
Caregivers in the intervention groups will undergo a four-session intervention program in addition to the routine care provided by other caregivers. The training, which is planned to last four weeks and includes activities aimed at reducing the impact of the caregiving role on caregivers, involves the delivery of a training program designed to improve caregivers' adaptation to their caregiving roles.
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.
Andre navne:
  • Social health dimension
  • Physical health
  • Psychological health dimension
  • Emotional health dimension

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Before intervention caregiving burden
Tidsramme: Before intervention

The Caregiver Burden Scale will be used to assess the stress experienced by caregivers.

It consists of 22 statements that evaluate the impact of caregiving on the caregiver's life and uses a Likert-type scale. The scale's highest score is 88, and the lowest is 0. Higher scores are associated with an increased caregiving burden.

Before intervention
After intervention caregiving burden
Tidsramme: 1 week after intervention
The Caregiver Burden Scale will be used to assess the stress experienced by caregivers. It consists of 22 statements that assess the impact of caregiving on the caregiver's life and uses a Likert-type scale. The maximum score on the scale is 88, and the minimum is 0. Higher scores are associated with increased caregiving burden.
1 week after intervention

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Before intervention
Tidsramme: Before intervention
Pre-Intervention Life Satisfaction This scale was developed to assess how an individual perceives their quality of life. The scale was created by condensing the World Health Organization Quality of Life Assessment scale to 26 questions. During the validity studies of the Turkish version, a national question was added, bringing the total number of questions to 27, and the Turkish version was finalized. Comprising closed-ended questions, the scale consists of the following subdimensions: general health, physical, social, environmental, and psychological. The minimum score that can be obtained from the scale is 0, and the maximum score is 100. An increase in the score indicates an improvement in quality of life.
Before intervention
After intervention
Tidsramme: 1 week after intervention
Post-Intervention Life Satisfaction This scale was developed to assess how an individual perceives their quality of life. The scale was created by condensing the World Health Organization Quality of Life Assessment scale to 26 questions. During the validity studies of the Turkish version, a national question was added, bringing the total number of questions to 27, and the Turkish version was finalized. Comprising closed-ended questions, the scale consists of the following subdimensions: general health, physical, social, environmental, and psychological. The minimum score that can be obtained from the scale is 0, and the maximum score is 100. An increase in the score indicates an improvement in quality of life.
1 week after intervention

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. juli 2026

Primær færdiggørelse (Anslået)

1. august 2026

Studieafslutning (Anslået)

1. august 2026

Datoer for studieregistrering

Først indsendt

8. maj 2026

Først indsendt, der opfyldte QC-kriterier

24. juni 2026

Først opslået (Faktiske)

26. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

26. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

24. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 10.01.2024-1389-1409
  • HF-24005 (Andet bevillings-/finansieringsnummer: Aydın Adnan Menderes University)

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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