- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03744299
The Interest of Cancer Patients and Caregivers in Acupuncture: a Survey (ACTIVATE)
February 20, 2019 updated by: Dr. Philip Debruyne, General Hospital Groeninge
Cancer and cancer treatments are accompanied by several possible side effects, such as nausea, hot flashes, fatigue, drowsiness, etc. Complementary and integrative therapies, such as acupuncture, could be used to manage these symptoms.
The aim of this study for our research team is to have an idea of the interest of cancer patients and caregivers in acupuncture.
This is a prospective, interventional study.
Cancer patients and caregivers will be approached at the day care clinic by a health care worker to participate in this study.
They will be asked to complete a questionnaire about their interest in acupuncture and their motivation, what symptoms they would need it for, where they would like this acupuncture to take place, whether they are willing to pay for it, and whether they would be interested in an information session about acupuncture.
Study Overview
Study Type
Interventional
Enrollment (Actual)
182
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Kortrijk, Belgium, 8500
- General Hospital Groeninge, Cancer Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Dutch speaking patients and caregivers
- Patients and caregivers presenting at the outpatient clinic, including the day-care clinic and follow up visits
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Intervention
Patients and caregivers are asked to complete a questionnaire
|
Patients and caregivers are asked to complete a questionnaire
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Response rate
Time Frame: At study inclusion
|
At study inclusion
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Interest in acupuncture assessed by questionnaire
Time Frame: At study inclusion
|
At study inclusion
|
Side effects participants would like to receive acupuncture for assessed by questionnaire
Time Frame: At study inclusion
|
At study inclusion
|
Place where an acupuncture treatment should take place assessed by questionnaire
Time Frame: At study inclusion
|
At study inclusion
|
Willingness to pay for an acupuncture treatment assessed by questionnaire
Time Frame: At study inclusion
|
At study inclusion
|
Interest in an information session about acupuncture assessed by questionnaire
Time Frame: At study inclusion
|
At study inclusion
|
Patient or caregiver characteristics (sex, age, diagnosis) collected by questionnaire
Time Frame: At study inclusion
|
At study inclusion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Philip Debruyne, MD, PhD, MSc, FRCP, General Hospital Groeninge
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 20, 2018
Primary Completion (Actual)
November 26, 2018
Study Completion (Actual)
November 27, 2018
Study Registration Dates
First Submitted
November 14, 2018
First Submitted That Met QC Criteria
November 14, 2018
First Posted (Actual)
November 16, 2018
Study Record Updates
Last Update Posted (Actual)
February 22, 2019
Last Update Submitted That Met QC Criteria
February 20, 2019
Last Verified
November 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- AZGS2018093
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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