Trial Radar KI | ||
|---|---|---|
enums.trial_summary.trial_summary_welcome | ||
Mother Screening for Relapse Using Mid-upper Arm Circumference Among Children Recovered From Severe Acute Malnutrition (Full Scale Trial) (MAMAN)
SPECIFIC AIM 1: Determine the effectiveness of training caregivers to screen for relapse to moderate acute malnutrition or severe acute malnutrition using mid-upper arm circumference tapes following recovery from severe acute malnutrition for improving anthropometric outcomes and improving time to relapse detection. It is hypothesized that caregiver screening will be effective for reducing time to detection of relapse and that children receiving caregiver screening will have better anthropometric measures at 6 months post recovery and faster time to detection of relapse among those who relapse.
- Specific Aim 1A: Determine if detection of relapse in children who have recently recovered from severe acute malnutrition is more expeditious when caregivers are trained to screen for relapse to moderate acute malnutrition or severe acute malnutrition using mid-upper arm circumference tapes compared to current standard of care. It is hypothesized that a reduction in time to relapse detection will occur when caregivers are trained to screen for relapse to moderate acute malnutrition or severe acute malnutrition using mid-upper arm circumference tapes.
- Specific Aim 1B: Determine the effectiveness of caregivers screening mid-upper arm circumference measurements on improving anthropometric outcomes for children. It is hypothesized that training for caregiver screening of mid-upper arm circumference will lead to earlier intervention and improved anthropometric outcomes for children at 12 months post-admission.
SPECIFIC AIM 2: Determine the acceptability caregiver mid-upper arm circumference training. It is hypothesized that most survey responses at the 3 and 6-month visits will show high levels of acceptance towards caregiver screening of children using mid-upper arm circumference tapes.
Mother Screening for Relapse Using Mid-upper Arm Circumference Among Children Recovered From Severe Acute Malnutrition (MAMAN)
- MAMAN
- 24-42418
Caregiver screening
malnutrition
home based malnutrition screening
| Teilnehmergruppe/Studienarm | Intervention/Behandlung |
|---|---|
Keine InterventionStandard of care treatment and follow-up schedule without alteration (control arm) This arm with serve as the control arm and receive the current standard of care, which is no caregiver training to conduct mid-upper arm circumference screenings and monthly clinic-based follow-up appointments for 3 months with a final visit at 6 months post enrollment. | Nicht zutreffend |
ExperimentellCaregiver mid-upper arm circumference (MUAC) screening and a standard of care follow-up schedule This arm will include caregiver screening with a mid-upper arm circumference tape at home weekly. Caregivers will be trained to screen their child for malnutrition relapse using mid-upper arm circumference tapes and requested to bring their child back to the clinic when relapse is detected. Additionally, this arm will receive the standard of care, which includes a monthly follow-up schedule for the first 3 months post enrollment and a final follow-up at 6 months. | Training Caregivers to Screen Children for Malnutrition Relapse Caregivers enrolled in the trial who are assigned to the two experimental arms, will be provided mid-upper arm circumference tapes and trained on how to screen their child for malnutrition relapse and asked to bring their child back to the clinic if relapse is detected. |
ExperimentellCaregiver mid-upper arm circumference (MUAC) screening and a reduced follow-up schedule This arm will include caregiver screening with a mid-upper arm circumference tape at home weekly. Caregivers will be trained to screen their child for malnutrition relapse using mid-upper arm circumference tapes and requested to bring their child back to the clinic when relapse is detected. Additionally, this arm will receive a reduced follow-up schedule at the clinic, which will include one planned visit at 3 months post enrollment and a final follow-up visit at 6 months. | Training Caregivers to Screen Children for Malnutrition Relapse Caregivers enrolled in the trial who are assigned to the two experimental arms, will be provided mid-upper arm circumference tapes and trained on how to screen their child for malnutrition relapse and asked to bring their child back to the clinic if relapse is detected. Reduced Follow-up Schedule Caregivers in one of the caregiver mid-upper arm circumference screening arms, will be asked to adhere to a reduced follow-up clinic visit schedule for when they bring their child to the clinic for planned visits. The standard of care includes monthly visits for the first 3 months post recovery, but those randomized to the reduced follow-up schedule arm, will not bring their child to the clinic for planned visits 1 month and 2 months after baseline. |
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Cumulative incidence of relapse | The primary outcome will be defined as the proportion of children who relapse to global acute malnutrition (either moderate acute malnutrition with mid-upper arm circumference \< 12.5 cm to ≥ 11.5 cm and/or weight-for-height Z score \< -2 to ≥ -3 or severe acute malnutrition with mid-upper arm circumference \< 11.5 cm and/or weight-for-height Z score \< -3) by the 6 month primary endpoint randomized by study assignment. | 6 months |
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Time to detection of relapse | The amount of time until the detection of malnutrition relapse will be assessed as a secondary outcome and will be defined as the time from the baseline visit until the planned or unplanned visit when malnutrition relapse is detected. This will be measured up until the 6 month visit and will be assessed by randomized study assignment. | 6 months |
Cumulative incidence of relapse to MAM or SAM separately | The proportion of children by randomized allocation who relapse to MAM or to SAM analyzed separately. | 6 months |
- Caregiver's aged 18 years old or older or a legal guardian or a relative aged 18 or older
- Child aged 6-54 months
- Child has recovered from an episode of severe acute malnutrition per Burkinabè national guidelines (weight-for-height ≥ -2 and/or mid-upper arm circumference ≥ 12.5 cm in the past month, with the criterion used for admissions corresponding to the original admission criteria)
- Family is planning to stay in the study area for 6 months
- Appropriate consent from the caregiver or guardian.
- Caregiver age under 18 years old, or legal guardian or relatives under 18 years old
- Child age < 6 months or > 54 months
- Twins/multiple births
- Children with feeding issues
- Did not recover from severe acute malnutrition in the past month
- Family is planning to move out of the study area in the next 6 months
- Caregiver or guardian refuses to provide consent
Centre de Recherche en Sante de Nouna, Burkina Faso
Thrasher Research Fund