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NOT YET RECRUITING
NCT07774416
NA

Feasibility, Acceptability And Usability Of The InControl Web Platform - A Rando Mized Parallel-Group Pilot Study of Mixed-methods

Sponsor: Aveiro University

View on ClinicalTrials.gov

Summary

This is a randomized, parallel-group pilot study that employs mixed methods (qualitative and quantitative approaches). The purpose of this study is to assess the feasibility, usability, and acceptability of an intervention with a digital component on the InControl web platform. The intervention is based on education in pain science and exercise, with the goal of managing chronic musculoskeletal pain in older adults. The intervention will be delivered through a combination of digital and in-person components and it will be compared to the usual intervention. It will also inform the design of a randomized controlled trial to evaluate the cost-effectiveness of InControl.

Official title: Feasibility, Acceptability And Usability Of The InControl Web Platform - A Mixed-methods Pilot Study

Key Details

Gender

All

Age Range

60 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

34

Start Date

2026-09

Completion Date

2026-12

Last Updated

2026-08-19

Healthy Volunteers

No

Interventions

OTHER

InControl intervention

The InControl intervention lasts 8 weeks and combines educational content on pain science and exercise on a digital platform. InControl is the result of a co-creation process between healthcare professionals and older adults with lived experience of chronic musculoskeletal pain.

OTHER

Usual Care

Usual care is defined as the treatment that the participant would normally receive such as medication, physical therapy, or any other form of treatment.