- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04844645
Using Mini Program for Self-management VS Conventional Pharmaceutical Care for Cancer Pain
Comparison of Cancer Pain Patients With or Without Mini Program
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Healthcare interventions delivered via personal mobile device have been shown to be acceptable to users, who have identified benefits such as convenience, access to personalized information, greater awareness of own health. Integrating mini program into the cancer pain care may be an effective strategy to improve cancer pain patients self-management.
To design, construct, and test the mini program in patients managing cancer pain, evaluate the total remission rate of pain and the improvement in medicine compliance to improve pain management for cancer pain patients, and assess patient acceptance of the mini program.
Studietype
Registrering (Forventet)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: QiuLing Zhao
- Telefonnummer: 5305 0591-83660063
- E-post: qlzhao8@163.com
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Patients aged 18 years or older;
- Be able to read Chinese and use a mobile phone;
- Histologically or cytologically confirmed solid tumor;
- Diagnosed chronic cancer pain
- Could understand the study process and evaluation, agreed to participate in the trial, and signed the informed consent form.
Exclusion Criteria:
- Illiterate person;
- Incompetence;
- Inability to complete the pain assessment;
- Participation in any other therapies or other study protocols that may have an impact on pain intensity, which were the main outcomes of this study;
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: a mini program trial group
Pharmacists conducted a standardized education session to teach the participants how to operate the mobile phone, use mini program, assess pain.
The participants in the trial group were asked to complete initial and final pain assessment questionnaires and Medication compliance on the mobile phones provided to them.
Participants were encouraged to use mini program as much as possible to record their pain status.
|
To design, construct, and test the mini program in patients managing cancer pain
Andre navn:
|
Sham-komparator: a control group
The control group received conventional pharmaceutical care.
Initial and final pain and Medication compliance data were collected.
Before the patient was discharged from the hospital, the clinical pharmacist conducted detailed medication education (including medication methods, prevention and treatment of adverse reactions, and precautions) and asked the patient to attempt to maintain a paper version of the pain diary.
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conventional pharmaceutical care
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Change in pain score
Tidsramme: Change from baseline at four weeks after discharge
|
Comparison of pain score of cancer pain patients with or without mini program.
Pain score will be assessed by using numeric rating scale (NRS).
An NRS allows a person to describe the intensity of his/her pain as a number usually ranging from 0 to 10, where "0" means "no pain" and "10" means pain as "bad as it could be."
|
Change from baseline at four weeks after discharge
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Change in medication adherence
Tidsramme: Change from baseline at four weeks after discharge
|
The investigators will measure the change in medication adherence via Morisky Scale.
Morisky Scale contains 4 questions, and the total score ranges from 0 to 4 with lower scores indicating higher adherence.
|
Change from baseline at four weeks after discharge
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Incidence of adverse events
Tidsramme: Up to four weeks after discharge
|
Adverse events will be assessed throughout the study according the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Event (CTCAE) Version 4.0.
Number of subjects who experienced an adverse event in this study is presented.
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Up to four weeks after discharge
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Change in quality of life
Tidsramme: Change from baseline at four weeks after discharge
|
Comparison of quality of life of cancer pain patients with or without mini program.
Quality of life is assessed using EuroQol- 5 Dimension (EQ-5D).
|
Change from baseline at four weeks after discharge
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Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Forventet)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- FJZLYX001
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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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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