Skip to content

Telerehabilitation Based on Aerobic Exercise in Fibromyalgia

Immediate Effects of a Telerehabilitation Program Based on Aerobic Exercise in Women With Fibromyalgia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04340674
Enrollment
34
Registered
2020-04-09
Start date
2020-02-06
Completion date
2020-10-19
Last updated
2020-11-03

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

Conditions

Fibromyalgia

Keywords

exercise, aerobic exercise, telerehabilitation

Brief summary

Fibromyalgia syndrome is the most common cause of chronic generalized musculoskeletal pain and is characterized by pain associated with generalizad sensitivity, fatigue, sleep disturbances and psychological problems. Due to the chronic nature of the pathology and the great dependence on analgesic drugs that it often entails, in these patients it is considered necessary to provide an individualized approach and provide strategies that allow symptoms to be controlled conservatively and non-pharmacologically. The objective of this trial is to analyse the immediate effects on pain, mechanical pain sensitivity, impact of fibromyalgia, pain catastrophizing, psychological distress and physical function when a telerehabilitation program based on aerobic exercise is applied in women with fibromyalgia. For this purpose the investigators conduct a randomized controlled trial single-blind (examiner). The investigators included female patients diagnosed of fibromyalgia according to the American College of Rheumatology (ACR). Thirty-four women with fibromyalgia are included and randomized into 2 groups: telerehabilitation program group based on aerobic exercise and control group. Exercise group receive 2 treatment sessions a week over 15 weeks. All the variables are measured at the beginning of intervention and after the intervention.

Interventions

OTHERTelerehabilitation based on aerobic exercise

To perform different whole body aerobic exercises moderately intense according to Borg scale.

Sponsors

University of Valladolid
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Women diagnosed medically with Fibromyalgia * Diagnosed according to the American College of Rheumatology criteria * Age between 30 and 75 years old * Telerehabilitation equipment including a laptop computer and access to internet

Exclusion criteria

* Any kind of contraindications for physical activity * Other physical or psychological therapies in the last 3 months. * Medication modifications in the last 3 months

Design outcomes

Primary

MeasureTime frameDescription
Pain IntensityBaselineThe investigators measure the intensity of pain with a Visual Analogic Scale at baseline. The scale score ranges from 0 to 100 and higher scores indicate greater pain intensity.

Secondary

MeasureTime frameDescription
Mechanical pain sensitivityBaselineThe investigators measure mechanical pain sensitivity of the 18 points described initially by the American College of rheumatology with an algometer at baseline
Pressure Pain ThresholdPost-intervention, an average 15 weeksThe investigators measure mechanical pain sensitivity of the 18 points described initially by the American College of rheumatology with an algometer at the end of treatment
Pain CatastrophizingBaselineThe investigators measure the pain catastrophizing with the Pain Catastrophizing Scale at baseline. Total values range from 0 to 52 points. Higher values indicate a higher level of pain catastrophizing.
Impact of fibromyalgia (Fibromyalgia Impact Questionnaire)BaselineThe investigators measure the impact of fibromyalgia with the Fibromyalgia Impact Questionnaire at baseline
Upper limb functionBaselineThe investigators measure upper limb functional capacity with the the Arm Curl Test at baseline. The number of repetitions that the participant can flex and re-extend the elbow holding a weight in 30 seconds is recorded.
Lower limb functionBaselineThe investigators measure lower limb functional capacity with the 6-Minute Walk Test at baseline. The distance (meters) that the patient can walk in 6 minutes is recorded.
Psychological distressBaselineThe investigators measure psychological distress levels with the Hospital Anxiety and Depression Scale at baseline.The questionnaire consists of two subscales and each subscale has a total score of 21 points. Higher scores represent higher levels of anxiety.

Countries

Spain

Outcome results

None listed

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