Enhancing SKIN Health and Safety in Aged CARE

Pressure Ulcer Clinical Trial

— SKINCARE  

Official title:

Enhancing SKIN Health and Safety in Aged CARE: An Exploratory Cluster Randomized Pragmatic Trial in Aged Nursing Home Residents (SKINCARE)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03824886
• Other study ID #: CRC-SP-A-30
• Status: Completed
• Phase: N/A
• Start date: October 1, 2018
• Est. completion date: June 4, 2021

Study information

• Verified date: August 2021
• Source: Charite University, Berlin, Germany
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Aged long-term care receivers are affected by various adverse skin conditions like pressure ulcers, incontinence-associated dermatitis, dryness, intertrigo and many more. Prevention of these skin problems and the provision of general hygiene and skin care activities are key areas of nursing practice. Numerous condition specific guidelines are available and are implemented separately. The more guidelines exist, the more difficult it is for nurses to implement them all. On the other hand, there is a huge overlap in terms of aetiology, pathogenesis and prevention of aforementioned skin conditions. The overall aim of this trial is to test the feasibility and to estimate possible effects of a comprehensive skin care package targeting main nursing relevant skin problems at the same time. Therefore a study will be performed in nursing homes of the state of Berlin comparing the skin care package to standard care. Residents' safety and subjective wellbeing will increase combined with improvements in professional competence of nurses. An advisory board consisting of international experts agreed already to supervise the trial.

Description:

Objectives and aims: Aged and care dependent patients suffer from many adverse skin conditions like xerosis cutis (including pruritus), pressure ulcers, skin tears, intertrigo and incontinence-associated dermatitis. Separate preventive strategies for these particular risks and diseases are available and partly implemented. Although distinct clinical diagnoses, there are substantial overlaps in terms of etiology (e.g. skin fragility, immobility) pathophysiology, prevention (e.g. safe handling, off-loading) and treatment (e.g. skin protection and care). Facilities are challenged to implement fragmented, condition-specific guidelines, neglecting shared etiologies and prevention and treatment principles, which has been shown to be an important barrier for implementation of evidence-based practice. Recently an evidence-based comprehensive skin care algorithm was developed. The objective of this trial is to investigate the feasibility of the implementation of this skin care package, to describe context factors for implementation, to estimate effect sizes and intracluster coefficients. Study design: An exploratory cluster randomized trial in aged nursing home residents will be conducted. The cluster design was chosen to avoid contamination between groups. A total of n = 500 residents from n = 20 nursing homes (randomly selected from the population of nursing homes of the state of Berlin) will be included in the study. In the intervention group (n = 10 nursing homes), the developed evidence-based algorithm will be implemented. The control group (n = 10 nursing homes) receives the usual standard care of the respective nursing home.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 405
• Est. completion date: June 4, 2021
• Est. primary completion date: June 4, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion/ Exclusion Criteria for Residents:

Inclusion Criteria:

• Living in the nursing home,
• 65+ years,
• 'Care degree 2' or higher according to SGB XI (Sozialgesetzbuch (Codebook of Social Law)),
• Written informed consent (by legal representative if required)

Exclusion Criteria:

• Residents at end of life,
• Any dermatological condition or skin affection requiring dermatological treatment,
• Known allergies to any product ingredients Inclusion/ Exclusion Criteria for Nursing Homes:

Inclusion Criteria:

• Nursing home in the federal state of Berlin with at least n = 70 or more residents.
• Expression of a clear commitment to implement the skin care algorithm if assigned to the intervention group,
• Valid pressure ulcer prevention standard/algorithm is in place,
• Written commitment to adherence to the trial procedures regardless of the outcome of

randomisation. Exclusion criteria:

• Nursing homes with less than n = 70 residents in the federal state of Berlin.

Exclusion Criteria:

• Nursing homes with less than n = 70 residents in the federal state of Berlin

Related Conditions & MeSH terms

• Dermatitis
• Dry Skin
• Incontinence-associated Dermatitis
• Intertrigo
• Pressure Ulcer
• Pruritus
• Skin Care
• Skin Tear
• Xerosis Cutis

Intervention

Other:
• Implementation of skin care algorithm
Implementation of structured and standardized skin care regimen

Locations

Country	Name	City	State
Germany	Charité - Universitätsmedizin Berlin	Berlin
Germany	Charité-Universitätsmedizin Berlin	Berlin

Sponsors (1)

Lead Sponsor	Collaborator
PD Dr. Jan Kottner

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of Pressure Ulcers (PU) Category II, III, IV, Unstageable, Deep Tissue Injury (DTI)	Proportions of newly developed PUs per person and per skin area to calculate the cumulative incidence	Week 12 +/- 1
Primary	Incidence of Pressure Ulcers (PU) Category II, III, IV, Unstageable, Deep Tissue Injury (DTI)	Proportions of newly developed PUs per person and per skin area to calculate the cumulative incidence	Week 24 +/- 1
Primary	Location of Pressure Ulcers (PU) Category II, III, IV, Unstageable, Deep Tissue Injury (DTI)	Classification according to NPUAP (National Pressure Ulcer Advisory Panel)/EPUAP (European Pressure Ulcer Advisory Panel) 2014	Week 12 +/- 1
Primary	Location of Pressure Ulcers (PU) Category II, III, IV, Unstageable, Deep Tissue Injury (DTI)	Classification according to NPUAP (National Pressure Ulcer Advisory Panel)/EPUAP (European Pressure Ulcer Advisory Panel) 2014	Week 24 +/- 1
Primary	Incidence of Incontinence-associated Dermatitis (IAD)	Proportions of newly developed IAD per person and per skin area to calculate the cumulative incidence. The classification of IAD will be according to GLOBIAD (Ghent Global IAD Categorisation tool) and distinction between intact and eroded skin according to Proceedings of the Global IAD Expert Panel.	Week 12 +/- 1
Primary	Incidence of Incontinence-associated Dermatitis (IAD)	Proportions of newly developed IAD per person and per skin area to calculate the cumulative incidence. The classification of IAD will be according to GLOBIAD (Ghent Global IAD Categorisation tool) and distinction between intact and eroded skin according to Proceedings of the Global IAD Expert Panel.	Week 24 +/- 1
Primary	Incidence of Intertrigo	Proportions of newly developed intertrigo per person and skin area to calculate the cumulative incidence. Medical diagnoses according to ICD (international classification of diseases) 11.	Week 12 ± 1
Primary	Incidence of Intertrigo	Proportions of newly developed intertrigo per person and skin area to calculate the cumulative incidence. Medical diagnoses according to ICD (international code of diseases) 11.	Week 24 ± 1
Primary	Incidence of Skin Tears (ST)	Proportions of newly developed STs per person and skin area to calculate the cumulative incidence. Classification according to ISTAP (International Skin Tear Advisory Panel).	Week 12 ± 1
Primary	Incidence of Skin Tears (ST)	Proportions of newly developed STs per person and skin area to calculate the cumulative incidence. Classification according to ISTAP (International Skin Tear Advisory Panel).	Week 24 ± 1
Secondary	Overall Dry Skin Score (ODS) on face, trunk, arms, hands, feet, legs	Change in Overall Dry Skin score. ODS is a clinical assessment of the presence and severity of skin dryness using a five-point scale. A score of '0' indicates no skin dryness, whereas a score of '4' indicates advanced skin roughness, large scales, inflammation and cracks.	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Stratum Corneum Hydration (SCH) measurements on right lower leg lateral, right midvolar forearm	Change in Stratum Corneum Hydration. SCH was measured using the Corneometer CM 825 (Courage + Khazaka, Cologne, Germany). This measurement is based on the differences of the dielectric constant of water and other substances. With this device, only the moisture content in the stratum corneum is measured. The arbitrary units (a.u.) range from 0 to 120 where as higher readings indicate higher stratum corneum hydration.; Means of triplicate measurements per skin area in arbitrary units at right lower leg lateral, right midvolar forearm; If measurements are not possible at right leg/arm (e.g. due to amputation) they will be conducted at contralateral skin areas	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Transepidermal Water Loss (TEWL) on right lower leg lateral, right midvolar forearm	Change in Transepidermal water loss. TEWL was measured with the Tewameter TM 300 (Courage + Khazaka, Cologne, Germany). The probe captures the constant permeation of water through the stratum corneum in gram per hour per m2. The measuring probe contains a pair of sensors that are located in different distances to the skin surface to determine temperature and relative humidity above the skin surface. The humidity gradient between both sensors is used for calculating the transepidermal water loss. Higher values indicate a higher transepidermal water loss.; Means of duplicate measurements per skin area in g/m2/h at right lower leg lateral, right midvolar forearm; If measurements are not possible at right leg/arm (e.g. due to amputation) they will be conducted at contralateral skin areas	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Skin Surface pH on right lower leg lateral, right midvolar forearm	Change in Skin surface pH. Skin surface pH was measured with the Skin-pH-Meter PH 905 (Courage + Khazaka, Cologne, Germany), a planar glass electrode. The pH is a measure of acidity and alkalinity of a solution and it indicates the concentration of the hydrogen ions in an aqueous solution. Reference values of human skin have been reported to range from 4 to 6.; Means of duplicate measurements per skin area at right lower leg lateral, right midvolar forearm; If measurements are not possible at right leg/arm (e.g. due to amputation) they will be conducted at contralateral skin areas	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Skin surface temperature [°C] on right lower leg lateral, right midvolar forearm	Skin surface temperature was measured with the Skin-Thermometer ST 500 (Courage+Khazaka electronic GmbH).; Means of duplicate measurements per skin area in °C at right lower leg lateral, right midvolar forearm; If measurements are not possible at right leg/arm (e.g. due to amputation) they will be conducted at contralateral skin areas	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Quality of Life (QoL) (residents without cognitive impairment): WHO-Five Well-being Index (WHO = World Health Organization)	Self-completion of the WHO-Five Well-being Index by residents without cognitive impairment. The German version of the WHO-Five Well-being Index questionnaire published by the World Health Organization in 1998 will be used. Scores range from '5' (all the time) to '0' (never) for in total five items.The sum scores range from 0, indicating the lowest well-being, to 25, indicating the highest well-being. A cut-off score of < 13 is recommended. Means will be calculated.; ? Means	Week 0, Week 24 ± 1
Secondary	Quality of Life (QoL) (cognitively impaired residents): QUALIDEM 18-Item Assessment (QUALIDEM = No original term, measurement instrument for proxy rating of quality of life in people with dementia)	The QUALIDEM assessment is a dementia-specific quality of life (QoL) instrument carried out by the nursing staff that allows a proxy-based QoL rating in all stages of dementia.The German version of the QUALIDEM version 2.0 published in 2015 will be used.Residents with a very severe dementia will answer the 18-item Instrument.To assess whether the resident is affected by mild to severe dementia or very severe dementia the global deterioration scale (GDS) will be used (see Outcome 22).	Week 0, Week 24 ± 1
Secondary	Quality of Life (QoL) (cognitively impaired residents): QUALIDEM 37-Item Assessment	The QUALIDEM assessment is a dementia-specific quality of life (QoL) instrument carried out by the nursing staff that allows a proxy-based QoL rating in all stages of dementia.The German version of the QUALIDEM version 2.0 published in 2015 will be used.In case the resident is affected by a mild to severe dementia the 37-item assessment will be used.To assess whether the resident is affected by mild to severe dementia or very severe dementia the global deterioration scale (GDS) will be used (see Outcome 22).	Week 0, Week 24 ± 1
Secondary	Itch Assessment	Self-completion of the 5-D itch scale by residents without cognitive impairment (according to GDS score of 1); The score of the 5-D Itch scale ranges from '5' (no pruritus) to '25' (most severe pruritus) and contains five items measuring pruritus over the past two weeks.; Means	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Pain Assessment (residents without cognitive impairment): numeric rating scale	? Self-completion of a numeric rating scale (NRS with total scores from 0: minimum pain to 10: maximum pain) to measure pain by residents without cognitive impairment. Means of the total score will be calculated.	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Pain Assessment (cognitively impaired residents): Verbal rating scale	? Verbal rating scale (proxy rated) to measure pain in cognitively impaired residents (VRS with total scores from 0: minimum pain to 10: maximum pain). Means of the total score will be calculated.	Week 0, Week 12 ± 1, Week 24 ± 1
Secondary	Assesment of dementia: Global Deterioration scale.	To assess whether the resident is affected by mild to severe dementia or very severe dementia the global deterioration scale (GDS) will be used. GDS scores from 2 to 6 indicate a mild to severe dementia and the 37-item assessment of the QUALIDEM tool will be used (see Outcome 18). A GDS score of 7 indicates very severe dementia and the 18-item QUALIDEM tool will be used (see Outcome 17).	Week 0