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Feasibility and Acceptability of Home-based Stretching Exercises in Fibromyalgia

Feasibility and Acceptability of Home-based Stretching Exercises in Patients With Fibromyalgia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06176053
Enrollment
12
Registered
2023-12-19
Start date
2024-02-15
Completion date
2024-05-30
Last updated
2024-06-28

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

Conditions

Fibromyalgia, Pain, Quality of Life

Brief summary

The study aims to gather knowledge about the patient's acceptance of the intervention and testing procedures, assess the adherence to the intervention, estimate the recruitment rate, and inform the sample size calculation for a subsequent randomized controlled trial.

Interventions

OTHERHomebased stretching exercise and app supervision

The intervention group will perform a self-administered, home-based stretching program (a total of 6 minutes per day) and maintain their daily activities as identified at baseline. Exercises are to be performed daily for six weeks. Adherence will be supported, and weekly contact with each participant will be maintained via a mHealth application.

Sponsors

Bispebjerg Hospital
CollaboratorOTHER
University of Copenhagen
CollaboratorOTHER
Aalborg University
CollaboratorOTHER
University College of Northern Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

Participants were blinded to the results of all measurements and naïve to research hypotheses.

Intervention model description

Feasibility and acceptability study

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Patients are included if they are aged 18 to 55 years and diagnosed with fibromyalgia in accordance with the American College of Rheumatology (ACR) criteria

Exclusion criteria

* Non-controlled systemic disorders * Impaired alertness or comprehension * relevant joint disorders (e.g., severe arthritis, arthroplasty of the hip or knee, and rheumatoid arthritis) * recent changes in therapy * neurological and musculoskeletal conditions that could compromise assessments

Design outcomes

Primary

MeasureTime frameDescription
Pressure pain thresholdsPressure pain thresholds were measured as a baseline before the participants are instructed in the home exercisesPressure pain thresholds was measures using a handheld pressure algometer

Secondary

MeasureTime frameDescription
Health related Quality of LifeQuality of life was measured as a baseline before the paticipants are instructed in the home exercisesQuality of life measured by the SF-36 Short Form
Range of motionRange of motion was measured as a baseline before the participants were instructed in the home exercisesPassive knee extension range of motion measured by the Biodex system 4 pro isokinetic dynamometer

Other

MeasureTime frameDescription
Fibromyalgia symptomsFibromyalgia symptoms were measured as a baseline before the paticipants are instructed in the home exercisesFibromyalgia symptoms were measure using the The Revised Fibromyalgia Impact Questionnaire (FIQR)

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026