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Severe Acute MalnutritionCRIMSONNCT06123390

Evaluating RISQ System Implementation in Acutely Malnourished Children in Chad (CRIMSON)

A study testing The Responses to Illness Severity Quantification (RISQ) System in people with Severe Acute Malnutrition, run by The Hospital for Sick Children at 1 site in Chad.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

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. Read more about this study

Who is it for?
Ages 6 to 59 months
Conditions the study is for
Severe Acute Malnutrition
What is being tested?
The Responses to Illness Severity Quantification (RISQ) System
Could I receive a placebo?
No, everyone receives an active treatment
How many people
14,671 participants
Where
1 siteChad
Study dates
11 Sep 2023to 9 Nov 2024
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 59 months
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Children:
  • age: 6 to 59 months at enrolment on the day of their admission/re-admission to the OptiMA program
  • written consent to participate
  • Front line staff providing care to patients enrolled in the Optima program:
  • [1] Registered Nurses [2] Medical Doctors

Who cannot join

  • Children:
  • Children allergic to milk, peanuts and/or ready-to-use therapeutic food (RUTF)
  • Children not residing in one of the study areas.

Trial locations and contacts

1 site in 1 country.

Chad1 site
  • Ngouri

    Ngouri

About this study

Official title: Cluster-Randomized Trial of the Implementation of the Responses to Illness Severity Quantification System (RISQ) in Children With Acute Malnutrition Six to Fifty-nine Months of Age in Ngouri, Chad

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.

Read the detailed description

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.

Being tested
The Responses to Illness Severity Quantification (RISQ) System
Keywords
decision support, mortality, illness severity, risk score
Medical subject headings
Severe Acute Malnutrition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • The Responses to Illness Severity Quantification (RISQ) SystemOther

    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 .

Study groups in NCT06123390
Study groupRoleWhat they receive
Usual CareNo interventionThe 17 health centres randomized to "Usual Care" will provide care as per OptiMA program.
Intervention ArmExperimentalThe 17 health centres randomized to the intervention arm will provide care as per OptiMA program with the addition of the RISQ System decision support.
Receives: Other: The Responses to Illness Severity Quantification (RISQ) System

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: 12 months

Secondary outcomes (8)
  1. 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

    Measured: Duration of hospitalization in days up to 60 days

  2. Timing of outpatient mortality

    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

    Measured: Duration of program inclusion in days up to 60 days

  3. Therapeutic intensity

    To be measured by location on admission to inpatient care (Intensive Care Unit/Phase1/Phase2)

    Measured: First 24 hours from admission to hospital

  4. Efficiency of inpatient care

    Efficiency measured by length of inpatient stay (whole or part days)

    Measured: Duration of hospitalization in days up to 60 days

  5. Workload

    Frontline staff perception of workload measured through questionnaires using a 5 point scale

    Measured: Month 1 and month 12

  6. Knowledge

    Frontline staff knowledge of assessment skills measured through questionnaire using a 5 point scale

    Measured: Month 1 and month 12

  7. 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

    Measured: 12 months

  8. Acceptability

    Acceptability of the RISQ System by front-line staff evaluated through a questionnaire using a 5 point scale

    Measured: Month 1 and month 12

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Nov 2023
  2. Study start11 Sep 2023
  3. Primary completion10 Sep 2024
  4. Study completion9 Nov 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
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.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
14,671 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06123390
Sponsor's protocol ID
1000080735
Acronym
CRIMSON
Status last verified
May 2026
First submitted
26 Oct 2023
Last updated
2 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: 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.

Publications

  • 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.

    PubMed 35582782
  • 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.

    PubMed 37419241
  • 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.

    PubMed 40462129

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