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| Name | Class |
|---|---|
| Alliance for International Medical Action | OTHER |
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The purpose of this study is to evaluate the effect of the Responses to Illness Severity Quantification (RISQ) system implementation on mortality and processes of care in a nutritional program treating children 6 to 59 months of age with acute malnutrition in Ngouri, Chad.
The CRIMSON Study is a 12-month cluster randomized trial that will evaluate the effect of implementing the RISQ system compared with usual care on all-cause mortality, in children with acute malnutrition aged 6 to 59 months enrolled in the OptiMA nutrition program in Chad.
The intervention is the RISQ System and the clusters are the individual health centres that are randomized with a ratio of 1:1, RISQ System: Usual care. The 12 month intervention period will begin following a run in phase in which sites randomized to intervention will introduce and establish the new practices and in which sites randomized to usual care will continue to provide usual care.
The RISQ system is a scientifically developed clinical decision support tool that consists of: [1] the RISQ score; [2] documentation form; [3] score-matched recommendations and [4] an implementation package. The RISQ score, developed through our prospective observational study in Maiduguri Nigeria ((NCT04582773) ranges from 0 to 26 (high scores indicating greatest severity of illness). In the development dataset, the mean RISQ score on admission was 3.6 in hospital survivors and 7.3 for children dying <48hr of admission. RISQ scores <24hr before death had Area Under the Receiver Operating Characteristics Curve (AUROC) of 0.93. The RISQ score performed similarly well in children independent of their clinical conditions as a diagnosis-independent measure of severity of illness. Additionally, through a study of 903 hospitalized children with Severe Acute Malnutrition (SAM), the RISQ score could discriminate between points of escalation or de-escalation of care and can reflect illness severity in children throughout hospitalization. The documentation form provides visual representation of the sub-scores of each RISQ score items and guidance for score calculation. The score-matched recommendations of the RISQ system that are linked to the RISQ scores are derived from an expert panel of clinicians, with over 100 years of collective experience caring for acutely malnourished children, and provide guidance about intensity of care. This includes the frequency of observation, consideration of secondary review, inpatient admission, and transfer into / out of inpatient care areas where more intensive treatments are provided.The implementation package consists of theoretical and practical training modules including specific 'train the trainers' sessions for key personal involved in the implementing programs.
The CRIMSON study is nested within the existing framework of the OptiMA nutritional program and observational study conducted by the Alliance for International Medical Action (ALIMA). The program involves health centres within Ngouri, a sub-prefecture of the Lake Region in Chad (and surrounding area) plus an inpatient unit at the Ngouri District Hospital providing care for children with acute malnutrition. Inclusion criteria for the OptiMA program are based on mid-upper arm circumference (MUAC) of <125mm and/or bilateral pitting oedema. Usual care in the OptiMA program is as follows: nutritional treatment to participants consists of Ready-to-use-Therapeutic Food (RUTF) adjusted based on their MUAC value throughout the duration of their care. Management of the children with acute illnesses follows the established approach for management of children with severe acute malnutrition using the World Health Organization (WHO) "danger signs" and Integrated Management of Childhood Illness (IMCI) algorithms to guide admission to hospital. Additionally, as part of the OptiMA program in Ngouri, pulse oximeters have been introduced in all health centres and inpatient care unit, following training by ALIMA. Included in the routine visits of the program is the measurement and documentation of each of the 7 RISQ score items [heart rate, respiratory rate, respiratory effort, oxygen saturation, temperature, level of consciousness and oxygen use (oxygen is currently only available in the inpatient care)] by nurses.
The investigators anticipate that implementation of the RISQ system in a nutrition treatment program will improve sensitivity and specificity of clinical evaluation in determining which children require hospitalization, and what level of medical care within the in-patient unit is appropriate and in turn potentially reduce mortality.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Usual Care | No Intervention | The 17 health centres randomized to "Usual Care" will provide care as per OptiMA program. | |
| Intervention Arm | Experimental | The 17 health centres randomized to the intervention arm will provide care as per OptiMA program with the addition of the RISQ System decision support. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| The Responses to Illness Severity Quantification (RISQ) System | Other | The RISQ System involves: [1] the RISQ score: calculated routinely using the [2] documentation record and linked to [3] score-matched recommendations. Introduction into clinical care is supported by [4] the RISQ System implementation package. During the 2 month prior to implementation, front-line staff in the intervention arm will be trained on and will practice the use of the RISQ System . |
| Measure | Description | Time Frame |
|---|---|---|
| All-cause mortality. | Mortality over the period beginning at admission to the program and ending at either program discharge or to a maximum of 60 days after study enrolment. Program discharge will be one of: [1] medical/anthropometric criteria or [2] defaulting from the program. Defaulting from the program is defined as children who do not attend the weekly clinic visits for 3 consecutive weeks. | 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Timing of inpatient mortality | Timing will be defined as [a] within 48 hours of hospital admission and [b] timing of death after admission to hospital | Duration of hospitalization in days up to 60 days |
| Timing of outpatient mortality |
| Measure | Description | Time Frame |
|---|---|---|
| Lived experience of RISQ System implementation | Lived experiences measured by open ended questions about strengths/weaknesses of RISQ System implementation added to frontline staff perception questionnaire at end of intervention period | one time at end of 12 month implementation period |
| comparison of automated versus manual measurements of vital signs (Respiratory rate in breaths/min) |
Inclusion Criteria:
Children:
Front line staff providing care to patients enrolled in the Optima program:
[1] Registered Nurses [2] Medical Doctors
Exclusion Criteria:
Children:
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| Name | Affiliation | Role |
|---|---|---|
| Christopher Parshuram, MD, PhD | The Hospital for Sick Children | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ngouri | Ngouri | Chad |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 35582782 | Background | Dale NM, Ashir GM, Maryah LB, Shepherd S, Tomlinson G, Briend A, Zlotkin S, Parshuram C. Development and an initial validation of the Responses to Illness Severity Quantification (RISQ) score for severely malnourished children. Acta Paediatr. 2022 Sep;111(9):1752-1763. doi: 10.1111/apa.16410. Epub 2022 Jun 3. | |
| 37419241 | Background |
| Label | URL |
|---|---|
| World Health Organization. Guideline: Updates on the Management of Severe Acute Malnutrition in Infants and Children \[Internet\]. 2013. | View source |
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On reasonable request - after publication of the study and with permission of parties attached to the study, and after Research Ethics Board review and approval.
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| ID | Term |
|---|---|
| D000067011 | Severe Acute Malnutrition |
| ID | Term |
|---|---|
| D044342 | Malnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
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| ID | Term |
|---|---|
| D016503 | Drug Delivery Systems |
| ID | Term |
|---|---|
| D004358 | Drug Therapy |
| D013812 | Therapeutics |
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In this study we are evaluating usual care (Arm 1) vs. the Responses to Illness Severity Quantification (Arm 2) in children children aged 6 to 59 months who are enrolled in the OptiMA nutrition program in Chad.
Community health centres will be the randomized clusters.
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The participants and care providers will know which arm of the study they are part of, as the randomization occurs at the facility level. Only the statistician will be blinded to the arms at the time of analysis.
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Timing will be defined as [a] within 48 hours of being seen by health-care team [b] timing of death after being seen by outpatient health-care team
| Duration of program inclusion in days up to 60 days |
| Therapeutic intensity | To be measured by location on admission to inpatient care (Intensive Care Unit/Phase1/Phase2) | First 24 hours from admission to hospital |
| Efficiency of inpatient care | Efficiency measured by length of inpatient stay (whole or part days) | Duration of hospitalization in days up to 60 days |
| Workload | Frontline staff perception of workload measured through questionnaires using a 5 point scale | Month 1 and month 12 |
| Knowledge | Frontline staff knowledge of assessment skills measured through questionnaire using a 5 point scale | Month 1 and month 12 |
| Fidelity of RISQ Implementation | Number of measured vital signs performed on individual patient at health centre visit with corresponding disposition in program, recorded in 10 randomly selected patients/week/health centre | 12 months |
| Acceptability | Acceptability of the RISQ System by front-line staff evaluated through a questionnaire using a 5 point scale | Month 1 and month 12 |
Comparison determined by agreement between the two different methods for respiratory rate measurement |
| During run-in phase prior to implementation of intervention, on average 2 months |
| comparison of automated versus manual measurements of vital signs (Temperature in degrees Celsius) | Comparison determined by agreement between the two different methods for temperature measurement | During run-in phase prior to implementation of intervention, on average 2 months |
| Comparison of RISQ scores among children with different clinical conditions in inpatient care | Differences in RISQ scores among children with different clinical diagnoses a) on admission to inpatient care; b) throughout inpatient care; and c) at exit from inpatient care | Duration of hospitalization in days up to 60 days |
| Dale NM, Ashir GM, Maryah LB, Shepherd S, Tomlinson G, Briend A, Zlotkin S, Parshuram CS. Evaluating the Validity of the Responses to Illness Severity Quantification Score to Discriminate Illness Severity and Level of Care Transitions in Hospitalized Children with Severe Acute Malnutrition. J Pediatr. 2023 Nov;262:113609. doi: 10.1016/j.jpeds.2023.113609. Epub 2023 Jul 5. |
| 40462129 | Derived | Dale NM, Hagre YD, Shepherd S, Tomlinson G, Zlotkin S, Ngaradoum M, Bechir M, Madjissem M, Tehoua C, Parshuram C. Cluster-randomized trial of the implementation of the Responses to Illness Severity Quantification (RISQ) system in children with acute malnutrition 6 to 59 months of age in Ngouri, Chad: the CRIMSON trial protocol. Trials. 2025 Jun 3;26(1):188. doi: 10.1186/s13063-025-08871-1. |
| World Health Organization. Pocket Book of Hospital Care for Children: Guidelines for the Management of Common Childhood Illnesses, 2013. | View source |
| World Health Organization. Handbook IMCI: Integrated Management of Childhood Illness \[Internet\]. 2005. | View source |
| Exploratory meeting to review new evidence for Integrated Management of Childhood Illness (IMCI) danger signs | View source |