An Adaptive Multi-arm Trial to Improve Clinical Outcomes Among Children Recovering From Complicated SAM

HIV Clinical Trial

— Co-SAM  

Official title:

Co-SAM: An Adaptive Multi-arm Trial to Improve Clinical Outcomes Among Children Recovering From Complicated Severe Acute Malnutrition

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05994742
• Other study ID #: 150522
• Status: Not yet recruiting
• Phase: Phase 3
• Start date: March 1, 2024
• Est. completion date: September 1, 2027

Study information

• Verified date: June 2023
• Source: Queen Mary University of London
• Contact: Isabella Cordani, BSc
• Phone: + 44 (0)2078822800
• Email: i.cordani[@]qmul.ac.uk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Malnutrition underlies 45% of child deaths, and has far-reaching educational, economic and health consequences. Severe acute malnutrition (SAM) affects 17 million children globally and is the most life-threatening form of malnutrition. Community-based management of acute malnutrition using ready-to-use therapeutic food (RUTF) has transformed outcomes for children with uncomplicated SAM, but those presenting with poor appetite or medical complications (categorised as having 'complicated' SAM) require hospitalisation. Data show that pneumonia, diarrhoea and malaria are leading causes of death in children with complicated SAM after discharge from hospital. High risk of infectious deaths suggests that sustained antimicrobial interventions may reduce mortality following discharge from hospital. Furthermore, children with complicated SAM respond less well to nutritional rehabilitation, and oftentimes are discharged to a home environment characterised by poverty and multiple caregiver vulnerabilities including depression, low decision making autonomy, lack of social support, gender-restricted family relations, and competing demands on scarce resources. Caregivers have to navigate diverse challenges that impede engagement with clinical care after discharge from hospital. The objective is to address the biological and social determinants of multimorbidity in children with complicated SAM by developing multimodal packages of interventions and testing them in a 5-arm adaptive randomized controlled clinical trial, with death/hospitalization or failed nutritional recovery as the primary outcome.

Description:

This is a 5-arm randomized, unblinded clinical trial comparing: Arm 1: Standard-of-care (control) Arm 2: Antimicrobial package Arm 3: Reformulated RUTF Arm 4: Psychosocial package Arm 5: Antimicrobial package + reformulated RUTF + psychosocial package The trial will test the superiority of each intervention arm over the standard of care arm (control). Children in the control arm (and all intervention arms) will receive RUTF for at least 2 weeks and all standard care. The trial is adaptive, meaning i) that each intervention arm will be added as it becomes available, and ii) an interim analysis will enable us to drop arms which are unpromising based on pre-specified criteria. There will be no blinding or placebo, because the very different components in each trial arm make it very challenging to blind. Children with complicated SAM will be screened and enrolled from hospital sites shortly before discharge, and interventions will be started before leaving hospital, and continued for 12 weeks through outpatient visits. Children will be followed at 2, 4, 6, 8, 12 and 24 weeks post-discharge in dedicated study clinics (with additional visits at 1, 3 and 5 weeks for caregiver-child pairs receiving the psychosocial intervention). The primary outcome is death or hospitalization or failed nutritional recovery by 24 weeks. The aim is to recruit 1266 children across three countries. The study is not testing new drugs but rather testing a different package of medications (Arms 2 and 5) as compared to current standard care, which the investigator believe will have greater benefit. The RUTF will be a new formula in two of the arms (3 and 5) based on research into what composition will improve health outcomes for children with complicated SAM. This will be a variant on Plumpy'Nut®, a brand that is known and trusted, produced in collaboration with the manufacturers, Nutriset. The Psychosocial intervention (Arms 4 and 5) will involve three components: i) The Friendship Bench, which was developed in Zimbabwe as a low-cost psychological intervention utilising problem-solving therapy (delivered by trained lay workers) and peer-to-peer support to address depression and other common mental disorders. There is a strong evidence-base for its use in urban LMIC settings. Peer support groups meet every 1-2 weeks and focus on communal problem solving, and establishing income-generation activities (such as making bags). ii) Care for Child Development is a UNICEF package that helps families build stronger relationships and solve problems in caring for the child at home, through play and communication activities to stimulate children, through a series of age-appropriate interactive modules delivered by a lay worker using 'flash' cards. It has been used in other African contexts and has good acceptability. iii) Educational and behavior-change messages around better nutrition; play for children with SAM; stigma, HIV and gender-based violence; financial planning; causes of SAM; and health-seeking behaviours. Blood and stool will be collected at baseline, 12 and 24 weeks from all children to explore recovery of underlying pathological processes. At week 2, liver function tests will be undertaken in local laboratories. Samples will also be transported to Kenya and the Netherlands for some assays not available in each country.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 1266
• Est. completion date: September 1, 2027
• Est. primary completion date: March 1, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Months to 59 Months

Eligibility

Inclusion Criteria:

• Age 6-59 months, of either sex
• Hospitalised with complicated severe acute malnutrition, as per WHO definition
• Started transition to RUTF
• Caregiver willing and able to attend the study clinic for all visits
• Caregiver able and willing to give informed consent

Exclusion Criteria:

• Any acute or chronic condition which mean that receipt of one or more study interventions, or participation in the trial, would not be advisable.

Related Conditions & MeSH terms

• Child Malnutrition
• Child Nutrition Disorders
• Comorbidities and Coexisting Conditions
• HIV
• Malnutrition
• Severe Acute Malnutrition

Intervention

Drug:
• Rifampicin
Rifampicin is commonly used in the first-line management of paediatric tuberculosis, and is approved by the FDA (ID: 2862628) and the EMA (EMA/31710/2020).
• Azithromycin
Azithromycin is a macrolide antibiotic, and is approved for use in children by the FDA (ID: 3263750) and EMA (EMA/2872/2021).
• Isoniazid
Isoniazid is an antibiotic commonly used in the firstline treatment of tuberculosis, and as tuberculosis prophylaxis.
• Pyridoxine Hydrochloride
Pyridoxine is a form of vitamin B6 used to prevent peripheral neuropathy among children receiving isoniazid.

Behavioral:
• The Friendship Bench
The Friendship Bench was developed in Zimbabwe as a low-cost psychological intervention utilising problemsolving therapy (delivered by trained lay workers) and peer-to-peer support to address depression and other common mental disorders. There is a strong evidence base for its use in urban LMIC settings. Peer support groups meet every 1-2 weeks and focus on communal problem solving, and establishing income-generation activities (such as making bags).
• Care for Child Development
Care for Child Development is a UNICEF package that helps families build stronger relationships and solve problems in caring for the child at home, through play and communication activities to stimulate children, through a series of age-appropriate interactive modules delivered by a lay worker using 'flash' cards. It has been used in other African contexts and has good acceptability.
• Educational and behaviour-change modules
Educational and behaviour-change messages around better nutrition; play for children with SAM; stigma,HIV and gender-based violence; financial planning; causes of SAM; and health-seeking behaviours. These have been developed with caregivers affected by SAM in a previous study, through a series of codesign workshops, ensuring these are contextually relevant.

Dietary Supplement:
• Reformulated Ready to Use Therapeutic Food
A reformulated product designed to improve outcomes for children who have severe acute malnutrition.

Other:
• Standard Care
All children will receive care according to WHO guidelines, which includes standard RUTF and any other medications required.

Locations

Country	Name	City	State
n/a

Sponsors (10)

Lead Sponsor	Collaborator
Queen Mary University of London	KEMRI-Wellcome Trust Collaborative Research Program, Kenya Medical Research Institute, National Institute for Health Research, United Kingdom, Tropical Gastroenterology & Nutrition Group (TROPGAN), University of Cambridge, University of Oxford, University of Washington, Wageningen University, Zvitambo Institute for Maternal & Child Health

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change in anthropometry: Weight-for-height Z score (WHZ)	Change in WHZ between baseline and 4 weeks post-randomisation, and baseline and 12 weeks post-randomisation.	4 weeks post-randomisation and 12 weeks post-randomisation
Other	Change in anthropometry: Weight-for-age Z score (WAZ)	Change in WAZ between baseline and 4 weeks post-randomisation, and baseline and 12 weeks post-randomisation.	4 weeks post-randomisation and 12 weeks post-randomisation
Other	Change in anthropometry: Height-for-age Z score (HAZ)	Change in HAZ between baseline and 4 weeks post-randomisation, and baseline and 12 weeks post-randomisation.	4 weeks post-randomisation and 12 weeks post-randomisation
Other	Change in anthropometry: Mid-upper arm circumference (MUAC)	Change in MUAC between baseline and 12 weeks post-randomisation.	4 weeks post-randomisation and 12 weeks post-randomisation
Other	Change in caregiver mental health	Change in Shona Symptom Questionnaire score (and proportion meeting cut-off score >8) between baseline and 24 weeks post-randomisation. This is a widely used 10-item self-report questionnaire. Each item is scored from 0-3, leading to a total score between 0-30, with higher scores indicating more severe depressive symptoms.	24 weeks post-randomisation
Other	Concentration of lipid mediators/proteins	LC-MS measurement of fatty acids, acylcarnitines, polyamines, amino acids, glycolysis intermediates, TCA cycle intermediates, nucleotides, prostaglandins, serotonin, bile acids, lysophosphatidylcholines, phosphatidylcholines, cholesterol and derivatives, organic acids and tri/di/monoglycerides.	12 weeks and 24 weeks post-randomisation
Other	Concentration of metabolites	Luminex measurement of Insulin, Insulin-like growth factor 1, leptin, ghrelin, cortisol, growth hormone, Glucagon-like peptide-1, Peptide YY, Monocyte chemoattractant protein-1, and Plasminogen activator inhibitor-1.	12 weeks and 24 weeks post-randomisation
Other	Concentration of inflammatory mediators	Luminex measurement of chemokines, cytokines and circulating growth factors.	12 weeks and 24 weeks post-randomisation
Primary	Mortality.	All-cause mortality.	24 weeks post-randomisation
Primary	Readmission to hospital.	Overnight admission to a health facility for any reason. This includes cases where there was a clinical plan to hospitalise the child, which was refused by the caregiver.	24 weeks post-randomisation
Primary	Failed nutritional recovery.	Failed nutritional recovery is defined as either: i) Persistent WHZ<-2 or MUAC<12.5cm or bilateral pedal oedema at week 12; or ii) WHZ<-2 or MUAC<12.5cm or bilateral pedal oedema at any time between baseline and week 24 post-randomisation in a child who had previously recovered.	24 weeks post-randomisation
Secondary	Change in weight-for-height Z-score	Change in weight-for-height Z-score between baseline and 24 weeks post-randomisation according to age- and-sex appropriate WHO reference standards.	24 weeks post-randomisation
Secondary	Change in mid-upper arm circumference	Change in size of mid-upper arm in centimetres between baseline and 24 weeks.	24 weeks post-randomisation
Secondary	Change in weight-for-age Z-score	Change in weight-for-age Z-score between baseline and 24 weeks post-randomisation according to age- and sex-appropriate WHO reference standards.	24 weeks post-randomisation
Secondary	Change in height-for-age Z-score	Change in height-for-age Z-score between baseline and 24 weeks post-randomisation according to age- and sex-appropriate WHO reference standards.	24 weeks post-randomisation
Secondary	Number of participants with suspected or confirmed tuberculosis,pneumonia, diarrhoea or malaria	Physician-diagnosed suspected or confirmed infection, as defined by WHO guidelines, between baseline and 24 weeks post-randomisation.	24 weeks post-randomisation