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Feasibility of a Real-world, Financial Psycho-oncology Intervention to Address Cancer-related Financial Distress

20. juli 2026 oppdatert av: Courtney Williams, University of Alabama at Birmingham

The goal of this pilot, feasibility study is to evaluate the feasibility and preliminary impact of a finance-specific psycho-oncology intervention, as well as to explore perceptions of and experiences with this financial psycho-oncology intervention for patients with cancer experiencing financial hardship. The main questions it aims to answer are:

  1. Is this financial psycho-oncology intervention feasible, acceptable, and appropriate for patients with cancer experiencing financial hardship?
  2. How can we refine the financial psycho-oncology intervention to best address financial distress for patients with cancer experiencing financial hardship?

Patients enrolled in the intervention will receive 2, 60-minute long, finance-specific psycho-oncology sessions per month over the course of 3 months, for a total of 6 sessions over the course of the intervention. Patients will complete surveys during intervention enrollment and after intervention completion to assess secondary outcomes of financial hardship, psychological distress, stress, and anxiety. Individuals who consent to the financial psycho-oncology intervention will also be invited to participate in a 30-minute semi-structured interview to explore their perceptions of and experiences with the financial psycho-oncology intervention, including concepts of participation and engagement, relevance and acceptability, content and understanding, logistics and practicality, and potential impact.

Studieoversikt

Status

Har ikke rekruttert ennå

Studietype

Intervensjonell

Registrering (Antatt)

20

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiekontakt

Studiesteder

    • Alabama
      • Birmingham, Alabama, Forente stater, 35233
        • University of Alabama at Birmingham
        • Ta kontakt med:
        • Hovedetterforsker:
          • Courtney Williams, DrPH

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

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  • Adult patients with cancer receiving treatment at the UAB Medical Oncology and/or UAB Supportive Care clinics

Exclusion Criteria:

  • non-English speakers
  • patients with non-melanoma skin cancers
  • patients with dementia/cognitive impairments

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Helsetjenesteforskning
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Patients receiving financial psycho-oncology intervention
Program which integrates emotional support, coping strategies, and financial psychoeducation to enhance patients' capacity to cope with both their emotional and financial burdens due to cancer.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Recruitment as a measure of feasibility
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
50% of contacted patients consenting to participate
From enrollment to the end of the financial psycho-oncology intervention at 3 months
Retention as a measure of feasibility
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
70% of consenting patients completing the program per protocol
From enrollment to the end of the financial psycho-oncology intervention at 3 months
Completion as a measure of feasibility
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
<15% missing survey data
From enrollment to the end of the financial psycho-oncology intervention at 3 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Financial hardship
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
as measured by COmprehensive Score for financial Toxicity (COST)
From enrollment to the end of the financial psycho-oncology intervention at 3 months
Change in Psychological distress
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
as measured by National Comprehensive Cancer Network Distress Thermometer and Problem List
From enrollment to the end of the financial psycho-oncology intervention at 3 months
Change in Perceived stress
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
as measured by Perceived Stress Scale (PSS-10)
From enrollment to the end of the financial psycho-oncology intervention at 3 months
Change in Anxiety
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
as measured by PROMIS Emotional Distress - Anxiety - Short Form 4
From enrollment to the end of the financial psycho-oncology intervention at 3 months
Change in Depression
Tidsramme: From enrollment to the end of the financial psycho-oncology intervention at 3 months
as measured by PROMIS Emotional Distress - Depression - Short Form 4
From enrollment to the end of the financial psycho-oncology intervention at 3 months

Samarbeidspartnere og etterforskere

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

Etterforskere

  • Hovedetterforsker: Courtney Williams, DrPH, University of Alabama at Birmingham

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)

1. mai 2027

Studiet fullført (Antatt)

1. august 2027

Datoer for studieregistrering

Først innsendt

16. juli 2026

Først innsendt som oppfylte QC-kriteriene

20. juli 2026

Først lagt ut (Faktiske)

23. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

23. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

20. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • PREP_Williams2026
  • UAB (Annen identifikator: UAB)

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

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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