Trying out treatments for chronic pain through personalised behavioural studies (Pilot study)

Overview
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StudyU allows you to use a scientific approach to personalise health-related activities and behaviours to better live with chronic pain in everyday life.

Sponsor: No sponsor defined

SEEK ID: https://ldh.hpi.imise.uni-leipzig.de/projects/7

Public web page: https://recover.centre.uq.edu.au/studyu-new-tool-self-manage-chronic-pain

NFDI4Health PIs: No PIs for this Trial Project

Trial Project start date: 12th Mar 2023

Extended Metadata (Nfdi4Health MDS 3.3)

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Resource classification(*)

Type of the resource(*) : Study

Title(s)/name(s) of the Project

Title/name(*) : Trying out treatments for chronic pain through personalised behavioural studies (Pilot study)
Language of the title/name(*) : English

Acronym(s) of the Project

Acronym(*) : CPPBS
Language of the acronym(*) : English

Description(s) of the Project

Description(*) : StudyU allows you to use a scientific approach to personalise health-related activities and behaviours to better live with chronic pain in everyday life.
Language of the description(*) : English

Keyword(s) describing the Project

Keyword(*) : chronic pain

Language(s) of the project : English

Web page of the project : https://recover.centre.uq.edu.au/studyu-new-tool-self-manage-chronic-pain

Contributor(s) of the Project

Is it a personal or organisational contribution?(*) : Organisational
Details about the contributing organisation(s)/institution(s)/group(s)
Contributor type(*) : Contact
Funding identifier(s) : Medibank Better Health Foundation, the Royal Australian College of General Practitioners and the Motor Accident Insurance Commission, Queensland
Name of the organisation/institution/group(*) : University of Queensland
Details about the contributing person(s)
Contributor type(*) : Contact
Given name(*) : Jane
Family name(s)(*) : Nikles
Digital identifier(s)
Identifier(*) : 0000-0001-5356-2291
Scheme(*) : ORCID
Email address : uqjnikle@uq.edu.au
Phone number : 0408599033
Organisation(s) associated with the contributor
Name(*) : University of Queensland
Address : Not specified
Web page : http://www.uq.edu.au/
Digital identifier(s)
Identifier(*) : 00rqy9422
Scheme(*) : ROR

Alternative identifiers

Type of the registry(*) : Not specified
Identifier(*) : Not specified

Includes chronic diseases? : true

Characteristics of the Project

Is it an interventional or non-interventional Project? : Interventional
Specification of the type of the Project
Interventional Project type : Crossover
Non-interventional Project type : []
Primary health condition(s) or disease(s) considered in the Project
Primary health condition or disease name(*) : Chronic pain
Terminology/classification(*) : ICD-10
Code of the health condition or disease : G89.4
Groups of diseases or conditions(*)
Which groups of diseases or conditions were the data collected on? : Diseases of the musculoskeletal system and connective tissue (XIII)
On which diseases or conditions were the data collected? : Lower level ICD-10 (https://icd.who.int/browse10/2019/en), with autocomplete
Collects mortality data? : No
Administrative information about the Project
Status of the ethics committee approval : Request for approval submitted, approval granted
Overall Project status : Ongoing (II): Recruitment and data collection ongoing
Participants enrolled by invitation? : Yes
Start date : 14 November 2024
End date : Not specified
Mono- or multicentric? : Multicentric
Number of centers : 4
One or more data providers? : Several data providers
Number of data providers : 1
Primary subject(*) : Person
Eligibility criteria for Project participants
Eligibility criteria: Minimum age
Minimum eligible age(*) : 18
Unit of age(*) : Years
Eligibility criteria: Maximum age
Maximum eligible age(*) : Not specified
Unit of age(*) : Not specified
Eligible gender : Male, Female, Diverse
Inclusion criteria : Over 18 years of age, have had pain affecting life for at least 3 months, have a mobile phone
Exclusion criteria : Not specified
Population of the Project(*)
Coverage : National
Country(ies) : []
Region(s) and/or city(ies) : Australia
Interventions of the Project
Name of the intervention(*) : Personalised exercise program
Type of the intervention : Behavioral (e.g., psychotherapy, lifestyle counseling)
Additional information about the intervention : Not specified
Name(s) of the arm(s) associated with the given intervention : Not specified
Exposures of the Project
Name of the exposure : Not specified
Type of the exposure : Not specified
Additional information about the exposure : Not specified
Name(s) of the group(s) associated with the given exposure : Not specified
Outcome measures in the Project
Name of the outcome measure(*) : Pain interference with general activity
Description of the outcome measure : Not specified
Type of the outcome measure : Primary
Time point(s) of assessment : Not specified
Additional information about the Project : Not specified
Additional assessments/measurements in the Project : Physical activity
Data sharing strategy of the Project(*)
Is it planned to share the data?(*) : Undecided, it is not yet known if data will be made available
Supporting documents available in addition to the data : []
When and for how long will the data be available? : Not specified
Criteria for data access : Not specified
Additional information about data sharing : Not specified
DataSHIELD/Opal infrastructure available? : No
Link to data request application : Not specified
Web page with additional information about data sharing : Not specified
Record linkage possible? : false
Non-interventional aspects of the Project
Temporal design : Prospective
Target follow-up duration of the Project
Target follow-up duration(*) : 8
Unit of time(*) : Weeks
Number of follow-ups conducted : 56
Biosamples retained in a biorepository : None retained
Specific types of retained biosamples : Not specified
Interventional aspects of the Project
Numerical phase : Not applicable
Masking of intervention(s) assignment
Masking implemented? : false
Who is masked? : []
Additional information about masking : Not specified
Type of allocation of participants to an arm : Randomized
Off-label use of a drug product : No

Annotated Properties

Topic annotations

Preclinical and clinical studies, Pain medicine

Trying out treatments for chronic pain through personalised behavioural studies (Pilot study)

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