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Comparison of Treadmill and Outdoor Walking in Patients With Fibromyalgia

Evaluation of the Effect of Open-Air Walking Supported by Treadmill and Mobile Application on Cardiopulmonary Function and Quality of Life in Patients With Fibromyalgia Syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07228897
Enrollment
54
Registered
2025-11-14
Start date
2025-12-05
Completion date
2026-11-01
Last updated
2026-02-24

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

Conditions

Fibromyalgia

Brief summary

While walking exercises performed outdoors are important within the scope of aerobic exercise, the continuity of outdoor walking exercises can be negatively affected by different weather conditions. Walking exercises performed indoors on a treadmill are a good option for patients in terms of increasing exercise continuity and patient compliance. Walking outdoors supported by a treadmill and mobile application may increase aerobic capacity and quality of life in patients with fibromyalgia syndrome, as well as reduce kinesiophobia.

Interventions

OTHERWalking exercises with treadmill

Patients will be enrolled in a treadmill exercise program in the cardiopulmonary exercise unit for 45 minutes, 3 days a week for 4 weeks.

OTHERWalking exercises at open air place

Patients will walk briskly outdoors for 45 minutes, 3 days a week for 4 weeks. Patients will receive notifications via a mobile app reminding them of their daily walk, and they will be asked to log their walks in the mobile app.

Sponsors

Ankara Etlik City Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

1. Be between the ages of 25 and 55 2. Be female 3. Have not engaged in regular physical activity for the past 3 months 4. Have been using the same medical treatment for at least 1 month prior to the study (amitriptyline, duloxetine/milnacipran, pregabalin, cyclobenzaprine) 5. Volunteering to participate in the study 6. The patient's cognitive status being suitable for using a mobile application 7. The patient agreeing to the 'Personal Data Protection Law Information Text' in order to use the mobile application

Exclusion criteria

1. History of cardiac or pulmonary disease 2. Changes in medical treatment during the study period 3. Use of different injection methods (ozone therapy, neural therapy, acupuncture, etc.) at least 3 months prior to the study or during the study period 4. History of rheumatological disease 5. Pregnancy or breastfeeding 6. History of malignancy 7. Presence of psychiatric or neurological disease

Design outcomes

Primary

MeasureTime frame
6-minute walk testFirst day of treatment, at the end of 4 week

Secondary

MeasureTime frame
Fibromyalgia Impact Questionnaire (FIQ)First day of treatment, at the end of 4 week
Measurement of maximum inspiratory and expiratory pressure (MIP) and (MEP)First day of treatment, at the end of 4 week
Beck Depression ScaleFirst day of treatment, at the end of 4 week
Fatigue Impact ScaleFirst day of treatment, at the end of 4 week
Short Form-36 (SF-36)First day of treatment, at the end of 4 week

Countries

Turkey (Türkiye)

Contacts

CONTACTAyşe Naz Kalem Özgen, Specialist
kalemnaz@gmail.com03127970000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026