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Effekten av latteryoga på individuelle og organisatoriske resultater hos sykepleieledere

18. september 2026 oppdatert av: SERPİL SUBAŞI ÇAĞLAR, Zonguldak Bulent Ecevit University

Effekten av latteryoga på individuelle og organisatoriske resultater blant sykepleiesjefer: En longitudinell studie

The goal of this clinical trial is to learn if laughter yoga can improve both individual and organizational outcomes in nurse managers. The main questions it aims to answer are:

  • Does laughter yoga lower burnout and stress levels in nurse managers?
  • Does laughter yoga improve work-life quality and job performance?
  • Does laughter yoga help nurse managers make better decisions and solve problems more effectively?
  • Does laughter yoga lower compassion fatigue and support positive approaches to workplace conflict? Researchers will compare a laughter yoga group with a control group to see if there are meaningful differences.

Participants will:

  • Join structured laughter yoga sessions for a defined period (weekly sessions).
  • Complete surveys before and after the program about stress, burnout, work-life quality, decision-making, problem solving, job performance, compassion fatigue, and conflict approaches.
  • Continue their usual work while attending sessions.

Studieoversikt

Detaljert beskrivelse

Nurse managers play a vital role in healthcare systems by ensuring the quality of nursing services, supporting staff, coordinating care, and solving organizational problems. However, the combination of administrative responsibilities, staff shortages, and high expectations often leads to stress, burnout, compassion fatigue, and difficulties in maintaining work-life balance. These conditions not only affect the individual health and well-being of nurse managers but also reduce team motivation, patient care quality, and overall organizational performance.

Laughter yoga is a mind-body practice that combines intentional laughter with breathing exercises. It does not rely on humor or jokes; instead, participants engage in guided group exercises that promote spontaneous and prolonged laughter. Scientific evidence suggests that laughter yoga can lower stress hormones, increase endorphins, improve mood, and strengthen social bonds. Although laughter yoga has been studied in various populations, there is a lack of randomized controlled trials (RCTs) specifically focusing on nurse managers and their professional challenges.

This randomized controlled trial aims to fill this gap by evaluating the individual and organizational outcomes of laughter yoga among nurse managers working in university and state hospitals.

The expected contribution of this study is to provide new evidence on a cost-effective, non-pharmacological intervention that can be easily integrated into hospital settings. If laughter yoga proves effective, it can be adopted as a sustainable strategy to support nurse managers' mental health, enhance their leadership capacity, and indirectly improve patient care and organizational outcomes.

Studietype

Intervensjonell

Registrering (Antatt)

80

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Currently working as a nurse manager
  • Having at least six months of managerial experience
  • Continuing to serve as a nurse manager throughout the study period

Exclusion Criteria:

  • Having previously received laughter yoga training
  • Use of medications affecting general health components during the study (e.g., for depression, anxiety)
  • Being pregnant
  • Experiencing an acute stressful life event, such as the death of a close relative
  • Having undergone abdominal surgery within the past 6 months

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Experimental: Laughter Yoga

Structured group-based laughter yoga sessions, 2 times per week, 30-45 minutes each, for 8 weeks.

This intervention consists of a structured Laughter Yoga Program designed for nurse managers. Each session includes breathing exercises, warm-up activities, guided and simulated laughter exercises (such as clapping, chanting, role-play laughter), and a short relaxation/meditation phase. Sessions are conducted in small groups by a certified facilitator. The program is delivered twice weekly for 8 weeks, with each session lasting approximately 30-45 minutes. The intervention is intended to reduce burnout, stress, and compassion fatigue, while improving decision-making, problem-solving, job performance, and work-life balance.

Andre navn:
  • Latterterapi;
  • Latterøvelser
Ingen inngripen: Control

Participants continue their routine work duties without any additional intervention.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Perceived Stress (Perceived Stress Scale - PSS)
Tidsramme: Baseline, 8 weeks, 3 months.

Developed by Cohen & Williamson, adapted to Turkish by Eskin in 2013. 14 items, single-factor measure of stress.

Scale Range: 0-56. Interpretation Higher scores = greater perceived stress (worse outcome).

Baseline, 8 weeks, 3 months.
Burnout Levels (Maslach Burnout Inventory - MBI)
Tidsramme: Baseline, immediately post-intervention (8 weeks), and follow-up (3 months after intervention).

Developed by Maslach & Jackson in 1986, adapted to Turkish by Ergin in1992. 22 items, three subscales: Emotional Exhaustion, Depersonalization, and Personal Accomplishment.

Scale Range: Emotional Exhaustion (0-54), Depersonalization (0-30), Personal Accomplishment (0-48).

Interpretation: Higher Emotional Exhaustion and Depersonalization scores = worse outcome; higher Personal Accomplishment scores = better outcome.

Baseline, immediately post-intervention (8 weeks), and follow-up (3 months after intervention).

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Problem Solving Inventory
Tidsramme: Baseline, 8 weeks, 3 months

Problem Solving Inventory, Developed by Heppner & Peterson in1982; adapted to Turkish by Şahin in 1993

Description: 31 items, six subscales: Problem-Solving Confidence, Approach-Avoidance, Personal Control, Planfulness, Impulsivity, Reflective Style.

Scale Range: 31-186. Interpretation: Higher scores = less effective problem solving (worse outcome); lower scores = better problem-solving skills.

Baseline, 8 weeks, 3 months
Work Performance
Tidsramme: Baseline, 8 weeks, 3 months.

Work Performance Job Performance Scale - Goodman and Svyantek in 1999; Turkish adaptation was made in 2014 by Bağcı.

Description: 25 items, two subscales: Task Performance and Contextual Performance.

Scale Range: 25-125. Interpretation: Higher scores = better work performance.

Baseline, 8 weeks, 3 months.
Compassion Fatigue
Tidsramme: Baseline, 8 weeks, 3 months

Developed by Dennis Portnoy and adapted Turkısh by Özdemir and Kutlu in 2022. The form consists of 40 items. The scale, which has no sub-dimensions, is evaluated based on the total number of items. The scale is a 3-point Likert-type scale: 1 = Very true, 2 = Partly true, and 3 = Rarely true. Those who answered "Very true" to 15 or more items in total are considered to have high levels of compassion fatigue.Cronbach alpha is 0,87

Baseline, 8 weeks, 3 months
Decision-Making Styles scale
Tidsramme: Baseline, 8 weeks, 3 months.

Developed by Scott and Bruce in 1995; adapted to Turkish by Yılmaz Kuşaklı in 2023

24 items, five subscales: Rational, Intuitive, Dependent, Avoidant, Spontaneous.

Scale Range: 24-120. Interpretation: Higher scores in each subscale = more frequent use of that decision-making style

Baseline, 8 weeks, 3 months.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. september 2026

Primær fullføring (Antatt)

17. desember 2026

Studiet fullført (Antatt)

17. mars 2027

Datoer for studieregistrering

Først innsendt

19. september 2025

Først innsendt som oppfylte QC-kriteriene

17. november 2025

Først lagt ut (Faktiske)

19. november 2025

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

21. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

18. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

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NEI

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Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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