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Hydrotherapy Intervention in Elderly With Knee Osteoarthritis

8-weeks Hydrotherapy Intervention in Patients With Knee Osteoarthritis.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02048956
Enrollment
34
Registered
2014-01-29
Start date
2014-01-31
Completion date
2016-08-31
Last updated
2016-11-02

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

Conditions

Knee Osteoarthritis

Keywords

knee osteoarthritis, hydrotherapy

Brief summary

Knee osteoarthritis is a common condition characterized by pain and functional disability in older people. Prevalence increases with age and is more frequent in older women. The aim of this study was to assess the effects of an 8-weeks hydrotherapy training with elastic bands on pain and functional disability in old people with knee osteoarthritis.

Detailed description

The main symptoms of knee osteoarthritis are pain and functional disability. These symptoms are caused by a progressive loss and deterioration of articular cartilage with reactive new bone formation at the joint's surface and margins involving articular cartilage, soft tissues and bone damage. Many treatment programs have been developed, including medication with nonsteroidal anti-inflammatory drugs, physical modalities, and therapeutic exercises. It is hypothesized that a hydrotherapy treatment during 8 weeks would benefit patients with knee osteoarthritis.

Interventions

OTHERHydrotherapy intervention

Participants randomized to the exercise programme received a training in a swimming pool focused on dance therapy.

OTHERControl group

Standard exercises of hydrotherapy

Sponsors

Universidad de Granada
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* confirmed clinical diagnosis of knee osteoarthritis

Exclusion criteria

* total knee arthroplasty * inability to co-operate or follow instructions. * a major neurological disorder

Design outcomes

Primary

MeasureTime frameDescription
Changes in pain pressure thresholdbaseline, 8 weeksThe pain pressure threshold is defined as the minimum amount of pressure necessary to induce pain or tenderness . It was measured using a pressure algometer (Somedic AB, Sweden), which is a device with a 1 cm diameter rubber disc at the end on quadriceps muscle.

Secondary

MeasureTime frameDescription
Changes in lower extremity strengthbaseline, 8 weeksChanges in the strength of lower limbs is going to be assessed using the Stairs Climbing Test. This test assesses the ability to ascend and descend a flight of stairs, as well as lower extremity strength, power, and balance.
Dual taskbaseline, 8 weeksDual task is going to be measured using the Timed Up & Go. It assesses basic mobility skill as well as strength, balance, and agility.
Functional abilitybaseline, 8 weeksFunctional ability was assessed by the Western Ontario and McMaster Universities Osteoarthritis Index. Higher scores on the this questionnaire represent greater limitations in function.
Changes in balancebaseline, 8 weeksThe in balance after the treatment is going to be assessed using the single leg stance. This is a clinical tool that is often used to assess balance and postural steadiness. Subjects are asked to lift one leg off the floor based on their preference and keep the leg raised as long as possible without touching the other leg or the floor

Other

MeasureTime frameDescription
Quality of sleepbaseline, 8 weeksQuality of sleep was assessed by Pittsburgh Sleep Quality Index, a self-reported questionnaire.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026