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A Multi-modal Approach to Addressing Cardiovascular Risk and Building Resilience in Youths With Psychosis (M3)

23. mai 2019 oppdatert av: Lynne Shinto, Oregon Health and Science University

Meals, Mindfulness & Moving Forward: A Multi-modal Approach to Addressing Cardiovascular Risk and Building Resilience in Youth Suffering From Psychosis

The purpose of this study is to determine the feasibility (≥ 50% completion rate) of a 6-week nutrition, movement, and mindfulness program for youth with recent diagnosis of psychosis.

Studieoversikt

Status

Fullført

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

The purpose of this study is to determine the feasibility of a 6-week nutrition, movement, and mindfulness program (M³ Program) for youth with a recent diagnosis of psychosis. Program effects on metabolic and mental health outcomes compared to wait-list control will also be assessed. Participants will be 15-25 years of age, and have a recent diagnosis of psychosis. Twenty participants and their study partners (20 study partners) will be equally divided into two cohorts. Participants will sign up for one of the two series on a rolling enrollment basis until both of the program date frames are filled. Participants that signed up for the second series will serve as a wait-list control; outcomes from the participants in the first series will be compared to this group. M³ will be a combination of didactic and experiential training. The course will meet once-a-week for six weeks. Participants will learn how to prepare healthy snacks and meals, make healthy choices when eating out, and interpret food packaging and labels. They will also learn about different forms of mindfulness exercises and movement, such as yoga, martial arts, and a Japanese style of drumming. Feasibility will be assessed throughout the program.

Studietype

Intervensjonell

Registrering (Faktiske)

33

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

  • Forente stater
    • Oregon
      • Portland, Oregon, Forente stater, 97239
        • Oregon Health and Science University

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

15 år til 25 år (Barn, Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • First diagnosis of psychosis occurs within 3 years of enrollment into the study or are a graduate of the Early Assessment and Support Alliance Program (EASA).
  • Established mental health provider and primary care physician.
  • Age 15 to 25 years (inclusive)
  • Able to enroll with a study partner (study partner can be a healthy volunteer)
  • Able to read and write in English

Exclusion Criteria:

  • Active suicidal or homicidal thoughts
  • Mental status exam which suggests high risk for disruptiveness to group process or danger to self and others.
  • If a graduate of EASA, the participant must have a primary care or mental health provider.

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Annen: M3 Program
Non-randomized experimental group. The program is a six-week multi-modal intervention, including nutrition education and cooking classes, physical activity, and mindfulness. Outcomes will be compared to a non-randomized control group.
Annen: M3 Program
Participants and their study partners will learn about food, movement, and mindfulness through hands-on curriculum.
Andre navn:
  • Meals, Mindfulness and Moving Foward Program
Annen: Control
Non-randomized control group. Outcomes will be compared at same time points (baseline, 6 weeks, 12 weeks).
Annen: Control
Participants will not participate in M3 program but will have same outcomes measured at same time points (baseline, 6 weeks, 12 weeks).

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Feasibility assessed by 6-week program completion by 50% of participants attending at least 60% of the program
Tidsramme: 6 weeks
6 weeks

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Body Mass Index
Tidsramme: 6 and12 weeks
body mass index
6 and12 weeks
Waist Circumference
Tidsramme: 6 and12 weeks
waist circumference measured in cm
6 and12 weeks
Lipid Panel
Tidsramme: 6 and12 weeks
total cholesterol, triglycerides, HDL, LDL
6 and12 weeks
Quick Scale for the Assessment of Negative Symptoms and Positive Symptoms
Tidsramme: 6 and12 weeks
A rating scale to measure positive symptoms of schizophrenia. The QSANS-QSAPS assessment is administered by a trained health professional and takes 30 to 45 minutes to complete.
6 and12 weeks
Connor-Davidson Resilience Scale
Tidsramme: 6 and12 weeks
A measurement of 'hardiness', or one's ability to successfully cope with stress. The scale draws on a number of resilient characteristics, including patience, tolerance to negative affect, sense of humor, commitment, recognition of limits to control, engaging the support of others, and adaptability. The CD-RISC contains 25 items and asks subjects to rate how they felt over the past month on a Likert-type scale. Total score range is 0 - 100, with higher scores indicating higher levels of resiliency.
6 and12 weeks
Quality of LIfe - SF12
Tidsramme: 6 and12 weeks
: The SF-12 is a 12-item validated shortened version of the SF-36 and was designed to provide a health related quality of life measure that was quick and easy to administer in large population studies. The SF-12 contains a subset of the 12 items from the SF-36 and information from this subset of questions is used to construct a physical and mental component summary score.
6 and12 weeks

Samarbeidspartnere og etterforskere

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Sponsor

Oregon Health and Science University

Etterforskere

  • Hovedetterforsker: Craigan Usher, MD, Oregon Health and Science University

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

1. februar 2015

Primær fullføring (Faktiske)

1. juli 2016

Studiet fullført (Faktiske)

1. juli 2016

Datoer for studieregistrering

Først innsendt

20. mars 2015

Først innsendt som oppfylte QC-kriteriene

24. mars 2015

Først lagt ut (Anslag)

25. mars 2015

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

28. mai 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

23. mai 2019

Sist bekreftet

1. mai 2019

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • 10376

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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