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NCT Number: NCT04605900

Impact of Therapeutic Footwear and Plantar Orthoses on Diabetic Neuropathic Foot in Quality of Life and Functionality

This study determines the effectiveness of plantar orthoses and custom-made orthopedic footwear in functional level and quality of life of persons with diabetes type 2 and diabetic peripheral neuropathy. This study is important due the loss of protective sensation, feet are vulnerable to minor trauma caused by plantar pressure as well as mechanical and thermal injuries. Thus, Plantar Orthoses become necessary to reduce PP and align the foot. Additionally, it is known that footwear is the most frequent cause of diabetic foot injury, since ulceration is frequently a consequence of the continuous trauma provoked by inadequate footwear. For a higher efficacy in the treatment of the foot, it is also necessary to use custom-made orthopedic footwear, indicated in the treatment of foot pathologies.

The lack of studies that evaluate the impact of this treatment on clinical measures such as quality of life and functional level, led to the development of this study, comparing a standard treatment (standard footwear and plantar orthoses) with an optimal treatment suggested in diabetic foot guidelines (therapeutic footwear and plantar orthoses).

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Key information

Conditions

Diabetes Mellitus, Type 2 Diabetes Mellitus Diabetic Peripheral Neuropathy Endocrine System Diseases Glucose Metabolism Disorders Metabolic Diseases Nutritional and Metabolic Diseases

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Marta Botelho

Faro, Algarve, 8005-139, Portugal

About this study

This clinical trial includes 2 parallel intervention groups with a pre- and post-test analysis. In the standard footwear (SF) group, plantar orthoses, standard footwear and education on foot self-care were applied and in the orthopedic footwear (OF) group the same intervention was applied, but with orthopedic footwear.

Both intervention groups were evaluated at two different time points, with the pre-test taking place at the beginning of the study (T0 - Baseline) and the post-test taking place 4 months after the application of the treatment (T4). In the middle of the study, at two months (T2) a questionnaire was applied in order to understand the adherence and the perception of individuals about the intervention applied.

The screening of diabetic peripheral neuropathy was made with the Michigan Neuropathy Screening Instrument (MNSI) and the description of the sample with an evaluation questionnaire.

The FL was evaluated through the Lower Extremity Functional Scale (LEFS), physical tests and the postural, static and dynamic barometric assessment. QoL was assessed with SF-36 and the adherence and satisfaction with a questionnaire created ad hoc.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Presence of type 2 DM;
  • Have at least 6 months from diagnosis of DM;
  • Presence of Diabetic Polyneuropathy;
  • No history of plantar orthoses and orthopedic footwear use.

Exclusion criteria

  • Active ulceration;
  • Severe osteoarticular deformities;
  • Presence of cognitive impairment;
  • Gait with technical devices;
  • Diagnosis of neurological pathology that can affect the gait pattern;
  • Diagnosis of another pathology that can negatively influence the study: depression, the presence of uncontrolled cardiovascular diseases and active cancer.
  • Surgical interventions on the spine and lower limbs, with less than 1 year of recovery.

Treatment and study plan

Orthopedic Footwear

Device

The orthopedic footwear used by the OF Group was manufactured by the company J. Andrade Ferreira Neves Lda. with materials suitable for the diabetic foot, as registered with INFARMED under registration ID 279515.

Standard Footwear

Device

In the SF Group, it was recommended to use standard shoes more suitable for diabetic foot, with some specific characteristics, such as sports or walking shoes. The acquisition or not of a more suitable shoes by the participants was at the discretion of each individual.

Plantar Orthoses

Device

The plantar orthoses (PO) that both groups used for distribute of plantar loads was based on the principle of total contact. The confection material consisted in a liner of EVA shore 20º and polyurethane filling ELAX flexible (expandable) from OKM Química Ortopédica SL.

Education on foot self-care

Behavioral

An information leaflet with foot care was delivered, with the aim of ensuring that participants were informed about the care they should continually take with their feet during the study period. This leaflet was created based on the guidelines of the "Associação Protetora dos Diabéticos" in Portugal.

Primary outcomes

  1. Change the Quality of Life

    Time frame: 4 months

    Significantly change any subscore or total score of Medical Outcomes Study 36-item Short-Form Health Survey instrument, that was use it to assess quality of life. Instrument scores can range between 0 - 100. Higher values mean better self-perception of quality of life.

  2. Change the Performance of Lower Extremity Functional Scale

    Time frame: 4 months

    Change at least 9 points in Lower Extremity Functional Scale (minimum change for clinically relevant functional improvement). Instrument scores can range between 0 - 80. Higher values mean better functionality.

  3. Change the Functional Reach Test performance

    Time frame: 4 months

    Significantly change the maximum distance (cm) attained in Functional Reach Test.

  4. Change the Unipedal Stance Test performance

    Time frame: 4 months

    Change the time (s) in left and right unipedal stance.

  5. Change the Static Full Tandem Test performance

    Time frame: 4 months

    Change the time (s) in full-tandem position.

  6. Change the Walking Full Tandem Test performance

    Time frame: 4 months

    Achieve at least 10 steps in full-tandem.

  7. Change the Time Up and Go Test performance

    Time frame: 4 months

    Change the time (s) in performing the Time Up and Go test.

  8. Change the 6 minutes walk test performance

    Time frame: 4 months

    Change the distance (m) covered for 6 minutes of walking.

Secondary outcomes

  1. Change the Postural Stability (length displacement of Center of Pressure)

    Time frame: 4 months

    Significantly change the length displacement (mm) of center of pressure.

  2. Change the Postural Stability (displacement of Center of Pressure)

    Time frame: 4 months

    Significantly change the amplitude mediolateral and anteroposterior displacement (mm) of Center of Pressure.

  3. Change the Postural Stability (Ellipse surface)

    Time frame: 4 months

    Significantly change the ellipse surface (mm2).

  4. Change the Postural Stability (Mean Speed of Center of Pressure)

    Time frame: 4 months

    Significantly change the mean speed of CoP (mm/s).

  5. Change the Postural Stability (Standard deviation of Center of Pressure)

    Time frame: 4 months

    Significantly change the mediolateral and anteroposterior standard deviation (mm).

  6. Change the Postural Stability (Root Mean Square)

    Time frame: 4 months

    Significantly change the root mean square index (mm).

  7. Change the Postural Stability (Romberg Ration Index)

    Time frame: 4 months

    Significantly change the romberg ration index (mm).

  8. Change the mean pressure in static position

    Time frame: 4 months

    Change the mean pressure (kPa) on each foot in static position.

  9. Change the maximum pressure in static position

    Time frame: 4 months

    Change the maximum pressure (kPa) in each forefoot and hindfoot in static position.

  10. Change the support surface in static position

    Time frame: 4 months

    Change the support surface (cm2) between the plantar surface and the platform sensors, during the support phase on each of the feet.

  11. Change the load distribution in static position

    Time frame: 4 months

    Change the load distribution (%) between each foot.

  12. Change the maximum pressure in gait

    Time frame: 4 months

    Change the maximum pressure (kPa) of each foot in gait.

  13. Change the mean pressure in gait

    Time frame: 4 months

    Change the mean pressure (kPa) on each foot in gait.

  14. Change the plantar impression length in gait

    Time frame: 4 months

    Change the plantar impression Length (mm) of each of the feet.

  15. Change the support surface in gait

    Time frame: 4 months

    Change the support surface (cm2) of each foot.

  16. Change the longitude of CoP in gait

    Time frame: 4 months

    Change the longitude of the center of pressure (mm) of each foot.

  17. Change the load distribution in gait

    Time frame: 4 months

    Change the load distribution (%) between the forefoot and hindfoot and between the medial and lateral zone.

  18. Change the foot progression angle of gait

    Time frame: 4 months

    Change the foot progression angle in gait.

  19. Change the double support time of gait

    Time frame: 4 months

    Change the double support time (ms) in gait.

  20. Change the support time of gait

    Time frame: 4 months

    Change the support time (ms) for each foot in gait.

  21. Change the step length of gait

    Time frame: 4 months

    Change the step length (m) in gait.

  22. Adherence to the intervention

    Time frame: 2 months

    Number of hours per day using the devices (telephone monitoring).

  23. Self-Perception of improvements

    Time frame: 2 months

    Presence or not of improvements in feet/legs with the devices (telephone monitoring).

  24. Satisfaction with devices

    Time frame: 2 months

    Level of Satisfaction (totally satisfied, quite satisfied, satisfied, little satisfied, dissatisfied) with the devices (telephone monitoring).

Sponsors and collaborators

Lead sponsor

Universidade do Algarve

Other

Collaborators

  • Associação para o Estudo da Diabetes Mellitus e de Apoio ao Diabético do Algarve (AEDMADA)
  • Instituto São João de Deus (ISJD)
  • Lola - J. Andrade Ferreira Neves Lda
  • OKM Química Ortopédica S.L.
  • Ortobalance - Ortopedia Técnica e Desportiva
  • Pierre Fabre Portugal
  • Sensor Médica
  • Unidade Funcional de Faro - Agrupamento de Centros de Saúde do Central
  • University of Huelva

Registry information

Official study title

Impact of Therapeutic Footwear and Plantar Orthoses for Patients With Diabetic Neuropathic Foot in Quality of Life and Functionality: A Interventional Study

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Oct 28, 2020
Registry last updated
Oct 30, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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