- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02785471
Assessing Online Interventions for Men's' Mental Health and Wellbeing
27. januar 2022 oppdatert av: Jodi Jacobson Frey, University of Maryland, Baltimore
The purpose of this study is to test a comprehensive, male-oriented, online screening and referral (Screening for Mental Health; SMH) and male-oriented online information and referral intervention program (Man Therapy; MT) to improve mental health and wellbeing with a focus on prevention of suicide and help-seeking behaviors among middle-aged men.
The online programs will be offered together to maximize the effect on reducing suicide behavior and increasing mental health help-seeking behaviors for men.
If successful in decreasing suicide behavior and ideation and increasing suicide help-seeking behavior, this intervention could be scaled up to contribute to a reduction in suicide behaviors and deaths across the country.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
554
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Maryland
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Baltimore, Maryland, Forente stater, 21201
- University of Maryland Baltimore
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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
25 år til 64 år (Voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Mann
Beskrivelse
Inclusion Criteria:
- men living in Michigan;
- 25-64 years of age at time of enrollment;
- scoring in the moderate- to high-risk range (or answering positively on Question 9) on the Harvard Department of Psychiatry/NDSD Scale (HANDS), scoring in the moderate- to high-risk range for anger on the DSM-5 Level 1 Cross-Cutting Symptom Measure, or identifying any risk for suicide ideation or behavior on the Columbia-Suicide Severity Rating Sale (C-SSRS); and
- fluent in reading English
Exclusion Criteria:
- females
- scoring in the low risk range on the Harvard Department of Psychiatry/NDSD Scale (HANDS), scoring in the low risk range for anger on the DSM-5 Level 1 Cross-Cutting Symptom Measure, or not identifying any risk for suicide ideation or behavior on the Columbia-Suicide Severity Rating Sale (C-SSRS); and
- not fluent in reading English
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Aktiv komparator: Screening for Mental Health only
Participants in the Screening for Mental Health only (control) group will complete the online depression and suicide screening and receive immediate feedback and referrals.
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Participants in the Screening for Mental Health (SMH)-only group will complete the online depression and suicide screening and receive immediate feedback and referrals.
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Eksperimentell: Screening for Mental Health & Man Therapy
Participants assigned to Screening for Mental Health & Man Therapy (intervention) group will be offered the Man Therapy program in conjunction with Screening for Mental Health.
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Participants assigned to Screening for Mental Health, plus Man Therapy (SMH+MT) group will be offered the Man Therapy program in conjunction with Screening for Mental Health.
MT provides online early intervention services designed specifically for men who are at risk for suicide and are less likely to engage in help-seeking behavior.
MT takes an innovative and humorous approach to mental health education and help seeking through a fictional "therapist" named Dr.
Rich Mahogany, who is a no-nonsense "man's man" who informs men about the importance of honest talk about life's challenges in addressing their problems.
The web portal allows review "manly mental health information, facts and tips," explore "man therapies," and view videos of men with lived experience.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Change in depression symptoms as measured by The HANDS: Harvard Department of Psychiatry National Depression Screening Day Scale
Tidsramme: Baseline; 2 weeks post randomization; 12 weeks post randomization
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Baseline; 2 weeks post randomization; 12 weeks post randomization
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Change in suicide risk as measured by the Columbia-Suicide Severity Rating Scale-Screen Version
Tidsramme: Baseline; 2 weeks post randomization; 12 weeks post randomization
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Baseline; 2 weeks post randomization; 12 weeks post randomization
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
change in attitudes toward help-seeking behavior as measured by the Attitudes Toward Seeking Professional Help short-form
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
|
2 weeks post randomization; 12 weeks post randomization
|
change in alcohol use/abuse as measured by the Alcohol Use Disorders Identification Test
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
|
2 weeks post randomization; 12 weeks post randomization
|
change in relationship conflicts as measured by the Psychological Aggression Scale
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
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change in financial situation as measured by two items (J1 and J4) of the 2009 National Financial Capability Study, Financial Industry Regulatory Authority
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
|
change in social support as measured by the Perceived Social Support and/or Conflict scale
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
|
change in interpersonal needs as measured by the Interpersonal Needs Questionnaire
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
|
2 weeks post randomization; 12 weeks post randomization
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change in drug use/abuse as measured by the National Institute of Drug Abuse Quick Screen
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
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change in physical aggression as measured by the Physical Aggression Index scale
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
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change in help seeking behavior as measured by the Perceived Stigma and Barriers to Care for Psychological Problems scale
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
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change in help seeking behavior as measured by the General Help Seeking Questionnaire
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
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change in physical and mental health as measured by the Healthy Days Measures
Tidsramme: 2 weeks post randomization; 12 weeks post randomization
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2 weeks post randomization; 12 weeks post randomization
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change in anger as measures by the DSM-5 Self Rated Level 1 Cross-Cutting Symptom Measure
Tidsramme: Baseline; 2 weeks post randomization; 12 weeks post randomization
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Baseline; 2 weeks post randomization; 12 weeks post randomization
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Jodi Jacobson Frey, University of Maryland, Baltimore
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. september 2016
Primær fullføring (Faktiske)
30. mai 2019
Studiet fullført (Faktiske)
31. august 2020
Datoer for studieregistrering
Først innsendt
6. april 2016
Først innsendt som oppfylte QC-kriteriene
24. mai 2016
Først lagt ut (Anslag)
27. mai 2016
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
10. februar 2022
Siste oppdatering sendt inn som oppfylte QC-kriteriene
27. januar 2022
Sist bekreftet
1. januar 2022
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- HP-00066262
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Nei
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
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Nei
produkt produsert i og eksportert fra USA
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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