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Exploring New Technologies to Manage Cancer Pain in the Community

20 gennaio 2016 aggiornato da: University of Aberdeen

Exploring the Desirability, Feasibility and Practicalities of Using Information and Communication Technology (ICT) to Improve Cancer Pain Management in the Community

This interview and focus group study will explore patient, caregiver, and health professional opinions about the potential roles of digital technology to support effective cancer pain management. The views, opinions, and ideas expressed in this study will be used to design and develop a digital intervention which is likely to take the form of a measurement (pain and analgesic use) guided medication management intervention to improve cancer pain management in the community.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Cancer is increasing in incidence and prevalence in the United Kingdom. Pain is the most frequent complication of cancer and cancer pain control is frequently suboptimal. Previous research has established several potentially modifiable reasons for suboptimal cancer pain management. These include: under-reporting of pain; inadequate communication about pain between patients and health care professionals ; inadequate assessment of pain by health care providers; inadequate analgesic prescribing; suboptimal adherence to prescribed analgesic regimens by patients; and failure to re-assess pain timeously.

Information and communication technology (ICT) is a term used to describe all digital technologies that facilitate the electronic capture, processing, storage, and exchange of information. ICT could offer innovative solutions to suboptimal cancer pain management. Technological solutions might include electronic diaries, available as applications or "apps", which could encourage pain self-monitoring by people with cancer, and prompt medical assessment when pain is poorly controlled. Accurate patient reported pain data could help professionals to adequately assess pain and might influence the patient-professional consultation. Feedback of adherence data to patients and carers might improve the way that medications are used. Electronic medication adherence devices are currently available which can capture data on analgesic utilisation and timing. This data might be useful for health care professionals to inform safe and timely adjustments of analgesic doses (i.e. is pain control poor because of inadequate analgesic dose or because of non-adherence to the prescribed regime?). The aim of the proposed study is to explore the desirability, feasibility, and practicalities of using ICT to improve cancer pain management The proposed study would seek the views of patients with cancer pain, their caregivers, and health care professionals, about using technology to help with cancer pain management. The study will investigate the acceptability of electronic pain diaries and electronic medication adherence devices to patients and health care professionals, barriers to using such technology, and how data generated from technology might be used by patients, caregivers, and health care professionals to improve cancer pain management. This study will form part of a programme of research and data from the proposed study will be used to inform the potential development of a technological intervention to improve the management of cancer pain in the community.

Tipo di studio

Osservativo

Iscrizione (Effettivo)

50

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Patients with cancer pain, their caregivers, and health care professionals.

Descrizione

Inclusion Criteria:

  • Patients

    • Adults, 18 years of age or over.
    • Established diagnosis of any cancer type.
    • Have experienced pain related to cancer or its treatment requiring any form of analgesic within the last three months.
    • Patients with all stages and grades of cancer who feel that they are willing and able to participate in an interview.

Caregivers • Caregivers aged 18 years of age or over who are or have been involved in providing care or assistance for somebody who has experienced cancer pain. Examples of caregivers might include family members, spouse, and close friends, who provide care and assistance to patients with cancer pain.

Professionals

• Registered doctors, nurses, and pharmacists who provide care for people with cancer pain.

Exclusion Criteria:

  • • Non- English language speakers. Qualitative investigations will be reliant on communication in English. Specific words and phrases will be analysed by English speaking researchers in order to identify thematic content. This study does not include resources for interpreting services.

    • Patients who are thought to have entered the terminal stages of their illness will be excluded. This will be judged at recruitment by the screening clinician from the patient's general practice. In the case that a recruited patient has become too ill to participate in the research or has died before participation, and a linked caregiver has expressed interest in the study, the caregiver will be contacted, offered sympathies, and will be given the opportunity to withdraw from the study or continue as planned. All conversations about the study will be conducted in a supportive manner that recognises the sensitivity of the subject matter.
    • Patients who are registered at Great Western Medical Practice, Aberdeen (Rosalind Adam, researcher and interviewer practices as a doctor there).
    • Any participant who declines to take part.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Patients with cancer pain
Qualitative semi-structured interviews with patients who have experienced cancer pain
Caregivers for those with cancer pain
Qualitative semi-structured interviews with caregivers who have cared for those who have experienced cancer pain.
Healthcare professionals
Healthcare professionals whose role involves the management of cancer pain.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Qualitative semi-structured interviews
Lasso di tempo: Eight months
Eight months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 febbraio 2015

Completamento primario (Effettivo)

1 agosto 2015

Completamento dello studio (Effettivo)

1 agosto 2015

Date di iscrizione allo studio

Primo inviato

14 gennaio 2015

Primo inviato che soddisfa i criteri di controllo qualità

16 gennaio 2015

Primo Inserito (Stima)

19 gennaio 2015

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

21 gennaio 2016

Ultimo aggiornamento inviato che soddisfa i criteri QC

20 gennaio 2016

Ultimo verificato

1 novembre 2015

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 2/069/14

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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