TY - JOUR
T1 - Aerobic exercise versus combined exercise therapy in women with fibromyalgia syndrome: a randomized controlled trial
AU - Sañudo, Borja
AU - Galiano, Delfín
AU - Carrasco, Luis
AU - Blagojevic, Milisa
AU - de Hoyo, Moisés
AU - Saxton, John
PY - 2010/12/1
Y1 - 2010/12/1
N2 - OBJECTIVE
To investigate the effects of supervised aerobic exercise (AE) and a combined program of supervised aerobic, muscle strengthening, and flexibility exercises (combined exercise [CE]) on important health outcomes in women with fibromyalgia syndrome (FMS).
DESIGN
Randomized controlled trial.
SETTING
Community-based supervised intervention.
PARTICIPANTS
Women (N=64) with a diagnosis of FMS according to the American College of Rheumatology criteria.
INTERVENTION
Participants were randomly allocated to 1 of 3 groups: supervised AE, supervised CE, or usual-care control. Exercise sessions were performed twice weekly (45-60min/session) for 24 weeks.
MAIN OUTCOME MEASURES
The primary outcome measure was the Fibromyalgia Impact Questionnaire (FIQ). Exploratory outcome measures were the 36-Item Short-Form Health Survey, Beck Depression Inventory (BDI), aerobic capacity (6-minute walk test), hand-grip strength, and range of motion in the shoulders and hips.
RESULTS
Compliance with both interventions was excellent, with women in the exercise groups attending more than 85% of sessions. A 14% to 15% improvement from baseline in total FIQ score was observed in the exercise groups (P≤.02) and was accompanied by decreases in BDI scores of 8.5 (P
AB - OBJECTIVE
To investigate the effects of supervised aerobic exercise (AE) and a combined program of supervised aerobic, muscle strengthening, and flexibility exercises (combined exercise [CE]) on important health outcomes in women with fibromyalgia syndrome (FMS).
DESIGN
Randomized controlled trial.
SETTING
Community-based supervised intervention.
PARTICIPANTS
Women (N=64) with a diagnosis of FMS according to the American College of Rheumatology criteria.
INTERVENTION
Participants were randomly allocated to 1 of 3 groups: supervised AE, supervised CE, or usual-care control. Exercise sessions were performed twice weekly (45-60min/session) for 24 weeks.
MAIN OUTCOME MEASURES
The primary outcome measure was the Fibromyalgia Impact Questionnaire (FIQ). Exploratory outcome measures were the 36-Item Short-Form Health Survey, Beck Depression Inventory (BDI), aerobic capacity (6-minute walk test), hand-grip strength, and range of motion in the shoulders and hips.
RESULTS
Compliance with both interventions was excellent, with women in the exercise groups attending more than 85% of sessions. A 14% to 15% improvement from baseline in total FIQ score was observed in the exercise groups (P≤.02) and was accompanied by decreases in BDI scores of 8.5 (P
U2 - 10.1016/j.apmr.2010.09.006
DO - 10.1016/j.apmr.2010.09.006
M3 - Article
SN - 0003-9993
VL - 91
SP - 1838
EP - 1843
JO - Archives of Physical Medicine and Rehabilitation
JF - Archives of Physical Medicine and Rehabilitation
IS - 12
ER -