- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07620990
Mindfulness Meditation in Hemodialysis Patients (MIND-HD)
1. juni 2026 opdateret af: Sevda Şahin, Cyprus Aydin University
The Effect of Mindfulness Meditation on Sleep, Stress, and Symptoms in Hemodialysis Patients: A Randomized Controlled Trial
This randomised controlled study aims to evaluate the effects of mindfulness meditation on sleep quality, perceived stress and symptoms levels ion hemodialysis patients.
Participants in the intervention group will receive a 4 week mindfulness meditation program in addition to routine care.
Outcomes will be assessed before and after the intervention using validated measurement tools.
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study is designed as a randomized controlled experimental trial conducted in hemodialysis units in Northern Cyprus.
Hemodialysis patients will be randomly assigned to intervention and control groups.The intervention group will participane in a structured 4 week mindfulness meditation program delivered through guided sessions, while the control group will continue receiving routine care.
The study aims to determine the effectiveness of mindfulness meditation on sleep quality, stress levels and symptoms management in hemodialysis patients.
Data will be collected before and after the intervention using validated assessment scales.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
50
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Sevda Sahin, RN, PhD Candidate
- Telefonnummer: +905488488005
- E-mail: sevda0584@hotmail.com
Studiesteder
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Famagusta, Cypern
- Rekruttering
- Famagusta State Hospital
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Kontakt:
- Sevda Sahin, RN, PhD Candidate
- Telefonnummer: +905488488005
- E-mail: sevda0584@hotmail.com
-
Kyrenia, Cypern
- Rekruttering
- Dr. Akçiçek State Hospital
-
Kontakt:
- Sevda Sahin, RN, PhD Candidate
- Telefonnummer: +905488488005
- E-mail: sevda0584@hotmail.com
-
Lefka, Cypern
- Rekruttering
- Cengiz Topel State Hospital
-
Kontakt:
- Sevda Sahin, RN, PhD Candidate
- Telefonnummer: +905488488005
- E-mail: sevda0584@hotmail.com
-
Nicosia, Cypern
- Rekruttering
- Dr. Burhan Nalbantoğlu State Hospital
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Kontakt:
- Sevda Sahin, RN, PhD Candidate
- Telefonnummer: +905488488005
- E-mail: sevda0584@hotmail.com
-
-
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:
- Patients aged between 18 and 75 years
- Patients receiving hemodialysis treatment for at least 3 months
- Patients with cognitive functions suitable for the intervention (dementia score ≥21)
- Patient without hearing, vision or communication problems
- Patients without a psychiatric diagnosis
- Patients able to use a smartphone or tablet
- Patients not participating in another study
- Patients not using sleep medication or antipsychotic drugs
Exclusion Criteria:
- Patients younger than 18 years or older than 75 years
- Patients receiving hemodialysis treatment for less than 3 months
- Patients with cognitive impairment unsuitable for the intervention (dementia score ≤21)
- Patient with hearing, vision or communication disabilities
- Patients diagnosed with psychiatric disorders
- Patients unable to use a smartphone or tablet
- Patients participating in another study
- Patients using sleep medication or antipsychotic drugs
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Mindfulness Meditation Group
Participants in this group will receive a 4 week meditation program in addition to routine hemodialysis care.
|
Participants in the intervention group will receive a 4 week mindfulness meditation program consisting of weekly guided mindfulness sessions and home practices.
The program is designed to improve sleep quality, reduce stress levels, and manage symptoms in hemodialysis patients.
|
|
Andet: Control Group
Participants in this group will receive rouyine hemodialysis care without mindfulness meditation intervention.
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Participants in the control group will receive routine care provided in the hemodialysis unit without mindfulness meditation intervention.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Pittsburgh Sleep Quality İndex (PSQİ) Score
Tidsramme: Baseline and 4 weeks after intervention
|
Pittsburgh Sleep Quality İndex (PSQİ) will be used to assess sleep quality in hemodialysis patients receiving mindfulness meditation intervention.
The total PSQİ score ranges from 0 to 21, with higher scores indicating poorer sleep quality.
|
Baseline and 4 weeks after intervention
|
|
Perceived Stress Scale (PSS) Score
Tidsramme: Baseline and 4 week after intervention.
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The Perceived Stress Scale (PSS) will be used to assess stress levels in hemodialysis patients receiving mindfulness meditation intervention.
Scores range from 0 to 40, with higher scores indicating higher perceived stress.
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Baseline and 4 week after intervention.
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Dialysis Symptom İndex (DSİ)
Tidsramme: Baseline and 4 weeks after intervention.
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TheDialysis Symptom İndex (DSİ) will be used to assess symptom burden in hemodialysis patients receiving mindfulness meditation intervention.
The total score ranges from 0 to 150, with higher scores indicating greater symptom burden.
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Baseline and 4 weeks after intervention.
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Sevda Sahin, RN, PhD Candidate, Cyprus Aydin University
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 (Faktiske)
15. april 2026
Primær færdiggørelse (Anslået)
1. juli 2026
Studieafslutning (Anslået)
1. august 2026
Datoer for studieregistrering
Først indsendt
26. maj 2026
Først indsendt, der opfyldte QC-kriterier
1. juni 2026
Først opslået (Faktiske)
2. juni 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
2. juni 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
1. juni 2026
Sidst verificeret
1. juni 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CAU-HD-MIND-2026
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
UBESLUTET
IPD-planbeskrivelse
Individual participant data sharing has not yet been determined.
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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Studerer et amerikansk FDA-reguleret enhedsprodukt
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