Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03220451
Other study ID # CE-17083
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 25, 2017
Est. completion date March 20, 2020

Study information

Verified date January 2021
Source Montecatone Rehabilitation Institute S.p.A.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

All patients with a significant deficiency of skin sensitivity and reduced mobility are potentially at risk of Pressure Ulcers (PUs), in particular the persons affected by Spinal Cord Injury (SCI), also due to their frequent alteration or loss of subcutaneous skin sensitivity. Pressure sores are one of the most common and fearful complications in SCI, with a severe impact on quality of life and on care health costs. They are often the cause of lengthening the time of hospitalization, slowing down clinical and rehabilitation programs and re-hospitalization. PUs, when arisen, heal slowly and, despite the protracted conservative medical therapies, sometimes they do not come to complete healing. Sometimes plastic surgery is needed, although even after it recurrence rates remain high. Further treatments have been proposed in addition to the usual medication, however they are characterized by a certain degree of invasiveness and are often conditioned by the availability of specific and sometimes expensive equipment, as well as by the presence of highly qualified personnel. In general, there is also a lack of good quality clinical trials for assessing their effectiveness and safety and they are often not decisive, especially for severe and recalcitrant ulcers. Among alternative techniques for the healing of skin ulcers in general, the adhesive elastic bandage, also known as "kinesio taping" and already recognized for the treatment of edema, hematoma and scarring, has been proposed. However, specific protocols and published studies are not available for PUs. The Montecatone Rehabilitation Institute, that hosts the largest Spinal Unit in Italy, pays great attention to the prevention and treatment of PUs in both acute and chronic patients. The rationale for the taping positioning around PUs investigated in this study is to improve lymphatic drainage and reactivation of the superficial bloodstream by increasing interstitial spaces and reducing skin and subcutaneous compression, notoriously compromised in the areas of onset of pressure sores. The total shortage in the literature and in user manuals of taping protocols for PUs supports this preliminary, exploratory, descriptive and uncontrolled pilot study with the primary aim of verifying the safety of a taping treatment for medium/severe grade PUs, "add-on" to the usual care. The choice of the ulcer sites selected (sacral and heel) has been affected by the feasibility of tape positioning.


Description:

All patients with a significant deficiency of skin sensitivity and reduced mobility are potentially at risk of Pressure Ulcers (PUs), in particular the persons affected by Spinal Cord Injury (SCI), also due to their frequent alteration or loss of subcutaneous skin sensitivity. More than one-third of individuals hospitalized in Spinal Units for rehabilitative treatments following a SCI develop PUs during acute hospitalization and it was also estimated that up to 85% of SCI persons develop at least one PU in the course of their lives. Pressure sores are therefore one of the most common and fearful complications in SCI, with a severe impact on quality of life and on care health costs. They are often the cause of lengthening the time of hospitalization, slowing down clinical and rehabilitation programs and re-hospitalization. PUs, when arisen, heal slowly and, despite the protracted conservative medical therapies, sometimes they do not come to complete healing. Sometimes plastic surgery is needed, although even after it recurrence rates remain high. Traditional treatment of PUs consists in the use of advanced dressings that may vary depending on the degree of staging of the lesion, its extent and the presence of clinical signs of necrosis and/or deep soft tissue infection. In addition to dressings, treatment cycles with intermittent negative pressure therapy can be indicated and the surgical approach (toilets + plastic reconstruction) could be reserved to chronic lesions with no response to traditional dressings or in the case of underlying osteomyelitis. Alternative treatments (e.g. electrotherapy, pulsed electromagnetic fields, ultraviolet light, infrared radiation, laser therapy, ultrasound, shock waves) have been proposed in addition to the usual medication, however they are characterized by a certain degree of invasiveness and are often conditioned by the availability of specific and sometimes expensive equipment, as well as by the presence of highly qualified personnel. In general, there is also a lack of good quality clinical trials for assessing the effectiveness and safety of such techniques that are often not decisive for healing, especially for severe and recalcitrant lesions. Among alternative techniques for the healing of skin ulcers in general, the adhesive elastic bandage, also known as "kinesio taping" or "neuro taping" and already recognized for the treatment of edema, hematoma and scarring, has been proposed. However, specific protocols and published studies are not available for PUs. The Montecatone Rehabilitation Institute hosts the largest Spinal Unit in Italy as for number of beds and patients admitted. In addition to the intensive rehabilitation of SCI patients, great attention is paid to the prevention and treatment of PUs in both acute and chronic patients, involving physicians, physiotherapists and nurses. Some Physical Therapists of the Hospital are trained and experienced in the use of adhesive elastic bandage for various neuromuscular applications and a physiotherapy/nursing team has conceived, under medical supervision, the taping protocol for the PUs therapy proposed in this study. The rationale for such a taping positioning around PUs is to improve lymphatic drainage and reactivation of the superficial bloodstream by increasing interstitial spaces and reducing skin and subcutaneous compression, notoriously compromised in the areas of onset of pressure sores. Therefore, it is considered that, thanks to the normalization of blood and lymphatic flow, the proposed protocol may have a facilitating action to heal such lesions, especially if they are severe and recalcitrant to normal therapies. The total shortage in the literature and in user manuals of taping protocols for PUs supports this preliminary, exploratory, descriptive and uncontrolled pilot study with the primary aim of verifying the safety of a taping treatment for medium/severe grade PUs, "add-on" to the usual care. The choice of the ulcer sites selected (sacral and heel) has been affected by the feasibility of tape positioning.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date March 20, 2020
Est. primary completion date March 20, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Spinal cord injury of any aetiology (traumatic and non-traumatic) and any neurological level, both complete and incomplete, occurred at least 3 months before; - Pressure ulcer occurred at least 1 month before; - Pressure ulcer staged III or IV, according to the National Pressure Ulcer Advisory Panel and European Pressure Ulcer Advisory Panel (NPUAP/EPUAP) classification; - Pressure ulcer located in sacral or heel region; - Pressure ulcer with cleansed bottom; - Stable clinical conditions; - Cognitive integrity and full collaboration of the subject. Exclusion Criteria: - Ulcerative skin lesion not due to pressure; - Pressure ulcer with frank signs of infection or suggestive of underlying osteomyelitis; - Eczema and/or irritated and/or psoriatic skin around the pressure ulcer; - Ongoing deep venous thrombosis; - Known allergy to elastic adhesive tape; - Ongoing neoplasia; - Uncompensated diabetes with signs of peripheral vasculopathy; - Evidence of peripheral polyneuropathy; - Circulatory problems (e.g. severe lower limb artery disease); - Significant respiratory problems (e.g. with ongoing assisted ventilation); - Ongoing sepsis; - Ongoing severe clinical instability; - Ongoing oral anticoagulant therapy; - Ongoing pregnancy.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Adhesive elastic taping
Adhesive elastic taping placed around a pressure ulcer, according to a planned placement technique

Locations

Country Name City State
Italy Montecatone Rehabilitation Institute S.p.A. Imola BO

Sponsors (1)

Lead Sponsor Collaborator
Montecatone Rehabilitation Institute S.p.A.

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Onset of possible adverse events due to the taping treatment Visual daily monitoring of possible adverse events, due to the adhesive elastic taping treatment Every day, during the 4-week tape application period
Primary Onset of possible adverse events due to the adhesive elastic taping treatment Visual daily monitoring of possible adverse events, due to the adhesive elastic taping treatment Every day, during the 4-week follow-up after the tape application period
Primary Onset of possible events hindering the healing of the pressure ulcer under investigation, due to the taping treatment Visual daily monitoring of possible events hindering the healing of the pressure ulcer under investigation, due to the adhesive elastic taping treatment Every day (during the 4-week tape application period)
Primary Onset of possible events hindering the healing of the pressure ulcer under investigation, due to the taping treatment Visual daily monitoring of possible events hindering the healing of the pressure ulcer under investigation, due to the adhesive elastic taping treatment Every day (during the 4-week follow-up after the tape application period)
Secondary Evolution of the characteristics of the pressure ulcer under investigation Pressure ulcer assessment with Bates-Jensen Wound Assessment Tool (BWAT), once a week Baseline (initial visit); once a week during the whole study period (12 weeks)
Secondary Evolution of the characteristics of the pressure ulcer under investigation Photographic shot of the pressure ulcer Baseline (initial visit); week 4; week 8; week 12
Secondary Patient's weight Patient's weight, in kilograms (kg) Baseline (initial visit)
Secondary Patient's height Patient's height, in meters (m) Baseline (initial visit)
Secondary Patient's Body Mass Index (BMI) Patient's BMI assessment (as one of the nutritional status indicators): Patient's weight and Patient's height are combined as kg/m^2 Baseline (initial visit)
Secondary Change in patient's blood hemoglobin Dosage of blood hemoglobin (as one of the nutritional status indicators): grams per deciliter Baseline (initial visit); week 4; week 8; week 12
Secondary Change in patient's blood number of lymphocytes: Dosage of blood number of lymphocytes (as one of the nutritional status indicators): billions per liter Baseline (initial visit); week 4; week 8; week 12
Secondary Change in patient's blood albumin Dosage of blood albumin (as one of the nutritional status indicators): grams per deciliter Baseline (initial visit); week 4; week 8; week 12
Secondary Change in patient's blood prealbumin Dosage of blood prealbumin (as one of the nutritional status indicators): milligrams per deciliter Baseline (initial visit); week 4; week 8; week 12
Secondary Change in patient's blood total proteins Dosage of blood total proteins (as one of the nutritional status indicators): grams per deciliter Baseline (initial visit); week 4; week 8; week 12
Secondary Change in patient's blood transferrin Dosage of blood total transferrin (as one of the nutritional status indicators): milligrams per deciliter Baseline (initial visit); week 4; week 8; week 12
Secondary Onset of patient's pain Pain assessment with Numeric Rating Scale (NRS), twice a day (morning and evening) during the whole study period (12 weeks) Baseline (initial visit); twice a day, during the whole study period (12 weeks)
Secondary Site of patient's pain (if any) Description of the site of possibly observed pain, twice a day (morning and evening) during the whole study period (12 weeks) Baseline (initial visit); twice a day, during the whole study period (12 weeks)
Secondary Change of patient's spasticity Spasticity assessment with the Modified Ashworth Scale (MAS) Baseline (initial visit); week 2; week 4; week 6; week 8; week 10; week 12
Secondary Tape employed for taping treatment Quantification of total tape employed for the taping application treatment for each pressure ulcer (in meters) End of tape application period (week 8)
Secondary Time-operator employed for taping treatment Quantification of total time-operator employed for the taping application treatment for each pressure ulcer (in minutes) End of tape application period (week 8)
See also
  Status Clinical Trial Phase
Active, not recruiting NCT06321172 - Muscle and Bone Changes After 6 Months of FES Cycling N/A
Completed NCT03457714 - Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial
Recruiting NCT05484557 - Prevention of Thromboembolism Using Apixaban vs Enoxaparin Following Spinal Cord Injury N/A
Suspended NCT05542238 - The Effect of Acute Exercise on Cardiac Autonomic, Cerebrovascular, and Cognitive Function in Spinal Cord Injury N/A
Recruiting NCT05503316 - The Roll of Balance Confidence in Gait Rehabilitation in Persons With a Lesion of the Central Nervous System N/A
Not yet recruiting NCT05506657 - Early Intervention to Promote Return to Work for People With Spinal Cord Injury N/A
Recruiting NCT04105114 - Transformation of Paralysis to Stepping Early Phase 1
Recruiting NCT03680872 - Restoring Motor and Sensory Hand Function in Tetraplegia Using a Neural Bypass System N/A
Completed NCT04221373 - Exoskeletal-Assisted Walking in SCI Acute Inpatient Rehabilitation N/A
Completed NCT00116337 - Spinal Cord Stimulation to Restore Cough N/A
Completed NCT03898700 - Coaching for Caregivers of Children With Spinal Cord Injury N/A
Recruiting NCT04883463 - Neuromodulation to Improve Respiratory Function in Cervical Spinal Cord Injury N/A
Active, not recruiting NCT04881565 - Losing Balance to Prevent Falls After Spinal Cord Injury (RBT+FES) N/A
Completed NCT04864262 - Photovoice for Spinal Cord Injury to Prevent Falls N/A
Recruiting NCT04007380 - Psychosocial, Cognitive, and Behavioral Consequences of Sleep-disordered Breathing After SCI N/A
Active, not recruiting NCT04544761 - Resilience in Persons Following Spinal Cord Injury
Terminated NCT03170557 - Randomized Comparative Trial for Persistent Pain in Spinal Cord Injury: Acupuncture vs Aspecific Needle Skin Stimulation N/A
Recruiting NCT04811235 - Optical Monitoring With Near-Infrared Spectroscopy for Spinal Cord Injury Trial N/A
Recruiting NCT04736849 - Epidural and Dorsal Root Stimulation in Humans With Spinal Cord Injury N/A
Active, not recruiting NCT05558254 - ROBERT® as an Intervention to Enhance Muscle Strength After Spinal Cord Injury N/A