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Treatment of forefoot problems in the elderly: a randomised trial of a standardised shoe & foot care advice in general practice versus podiatric treatment

Treatment of forefoot problems in the elderly: a randomised trial of a standardised shoe & foot care advice in general practice versus podiatric treatment - Treatment of forefoot problems: shoe advice versus podiatric tratment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON32489
Enrollment
200
Registered
2009-12-02
Start date
2010-02-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

bewegingsapparaat: voeten forefoot problems forefoot complaints

Interventions

usual care podiatric treatment will be compared to the advice to wear fitting good quality shoes . This advice is supported by a information leaflet.

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Forefoot problems are caused by musculoskeletal conditions or deformities; Patients who indicate actual pain in the forefoot for a period of at least 1 months; Patients report disability as a result of the foot problem; Patients are able to fill in the questionnaires (if needed with help of others); Informed consent.

Exclusion criteria

Exclusion criteria: The problem is caused by a recent trauma of the foot; previous foot operation; Treatment of the foot problem by a podiatrists, pedorthist or a physiotherapist in the previous year;Rheumatoid arthritis;Terminally ill or too frail to participate; Known to have dementia;Diabetes mellitus with reduced foot sensation secondary to peripheral neuropathy

Design outcomes

Secondary

MeasureTime frame
Secondary outcome measures include foot function, self perceived deformity and perceived benefit. A process evaluation will be performed in all patients by questionnaire after 3 and 12 months in which the adherence to the given advice and treatment will be assessed. In addition an expert team will perform an evaluation of the treatment in the podiatric treatment group and the effect of orthosis treatment on in-shoe plantar pressure will be evaluated in a sample of 25 of these patients.

Primary

MeasureTime frame
For the primary aim of this study validated outcome measures will be assessed at 3, 6, 9 and 12 months using postal questionnaires. The primary outcome measures are: foot-related disability; severity of foot pain and limitations at work and other social activities.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)