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Pain in Cancer Patients.

Implementing the Dutch guideline "Pain in Cancer Patients".

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21593
Enrollment
210
Registered
2011-02-01
Start date
2010-12-15
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

aandoening: patients with cancer and pain (kanker en pijn) The incidence and prevalence of cancer is high, and many cancer patients have pain. The next decade, the prevalence of patients with cancer and oncological pain will still increase, so knowledge of barriers and misbeliefs of caregivers and patients about pain reporting, diagnosing and treating pain, together with improved communication is of upmost importance.

Interventions

Multifaceted intervention: 1. In-person training in the most important aspects of the guideline (including 2 repeating sessions) (in total three sessions of one hour- few hours) of medical oncologist
2. Interactive computer-based training (once) in the most important aspects of the guideline will be offered to general praticitioners
3. Pateints recieve SMS-alerts once a week to ask for their pain (NRS score). If patients have an NRS score of 5 of higher a nurse will contact the patient and the patient will recieve a personal advi

Sponsors

Universitair Medisch Centrum St Radboud te Nijmegen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants: Via the hospital boards, professional caregivers, oncologists and nurses involved in cancer care of the six participating hospitals will be invited to take part. Patients who visit the oncology outpatient clinic will be screened for possible inclusion. Patients will be invited to take part by their medical oncologist or research nurse if they experience pain for the first time caused by cancer. Overall inclusion criteria for patients are: 1. Diagnosed with cancer; 2. Aged 18 years or older; 3. Pain intensity of 3 or more on an numeric rating scale (NRS) for the worst pain experienced in the last 24 hours; 4. Having and being familiar with the use of a mobile phone.

Exclusion criteria

Exclusion criteria: 1. Dementia and other severe cognitive disorders; 2. No informed consent; 3. Not Dutch speaking and writing.

Design outcomes

Primary

MeasureTime frame
1. Percentage of all patients that visit the medical oncology outpatient clinic with adequate pain therapy/medication with the Pain Management Index (PMI); 2. Mean pain intensity of those cancer patients with pain (NRS).

Secondary

MeasureTime frame
1. Percentage of medical records of new patients in the outpatients oncology clinic, in which pain is registered with NRS; 2. Quality of life of patients with pain (EORTC QLQ-C30); 3. Knowledge of doctors of content of the guideline (questionnaire and Vignette); 4. Prospective descriptive study of pain intensity of the group of patients that will be monitored via sms-alerts and SMS pain reporting; 5. Process evaluation of the intervention study.

Contacts

Public ContactNienke Boveldt, te

Huispost 630, route 598 postbus 9101

n.teboveldt@umcn.anes.nl+31 (0)24 3617389

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)