Effectiveness of a Positive Deviance Program in Reducing Childhood Undernutrition
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| ClinicalTrials.gov Identifier: NCT04688515 |
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Recruitment Status :
Not yet recruiting
First Posted : December 30, 2020
Last Update Posted : September 29, 2021
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Malnutrition, Child | Behavioral: Nutrition program developed using positive deviance approach | Not Applicable |
Background:
Undernourished children who fail to grow in height and weight as other normal children can be underweight, stunting or wasting. In fully urbanized area such as Kuala Lumpur in Malaysia, the consequences of undernutrition are more detrimental in urban poor young children. Since young children are generally depending on maternal feeding for daily diet, alternative intervention that focus on encouraging positive change in maternal behaviour when feeding children might be efficient in reducing childhood undernutrition. The positive deviance (PD) approach is one such alternative intervention. This approach emphases the identification of positive deviant, individuals who successfully discover a way to solve a problem by performing some uncommon but advantageous actions or behaviours in the same underprivileged environment as their peers. In the context of child nutrition, positive deviance is more frequently referred to as adaptive child care practices, positive hygiene practices and feeding practices that enable children to develop appropriately in a harsh environment with limited resources. The nutrition program developed using this approach helps to discover positive deviant, spread local wisdom from mothers of well-nourished children to mothers of undernourished children, and initiate positive behavioural change as a preliminary step to promote healthy weight gain in children.
Methods:
This is a mixed method study which will be carried out in two phases. Phase I of the study will involve focus group discussion (FGD) with semi-structured interview to explore maternal feeding practices and also foods being fed to children. Mothers of children aged 3 to 5 years old will be recruited through purposive sampling or until saturation point is reached. Phase II of the study will involve a two-armed randomized controlled trial to evaluate effectiveness of nutrition program. A total of 164 mother-child dyads will be recruited, in which 82 of them will be recruited separately and randomly from different PPR flats with 1:1 allocation to form intervention and comparison groups. Ethical approval will be obtained from the Ethics Committee for Research Involving Human Subjects Universiti Putra Malaysia (JKEUPM). Permission to conduct this study in PPR flats and the list of PPR flats in KL will be obtained from the Kuala Lumpur City Hall. Intervention group will need to participate in a nutrition program for 3 months that consists of education session with peer-led cooking session and rehabilitation session. The comparison group will be given all the materials used in the program for reference after the last data collection. The height and weight of children will be measured by researcher. Mothers will be interviewed on the dietary intake of their children. Mothers will also need to answer a Malay language self-administered questionnaire to obtain information on socio-demographic characteristics, nutrition knowledge and food security status. These measurements will be taken at the baseline (before intervention), immediate post-intervention and 3-month post-intervention for both intervention and comparison groups.
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 164 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Effectiveness of a Nutrition Program Using Positive Deviance Approach to Reduce Undernutrition Among Urban Poor Children Under Five in Kuala Lumpur, Malaysia: A Two-armed Cluster Randomized Controlled Trial |
| Estimated Study Start Date : | January 2022 |
| Estimated Primary Completion Date : | March 2022 |
| Estimated Study Completion Date : | December 2023 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Intervention group
Intervention group refers to mother-child dyads who will be participating in a nutrition program consisting of nutrition education and cooking sessions for 3 months.
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Behavioral: Nutrition program developed using positive deviance approach
It is a 3-month nutrition program including nutrition education session and rehabilitation session. The education session consists of half hour education lesson and one and half hours peer-led cooking session. The cooking demonstration will be led by volunteers from PD family. Participating mothers will need to bring along their children during this session, prepare meal according to pre-planned menu and feed their children with the prepared meal after cooking as snack or additional meal. The rehabilitation session will be the rest of the days following each education session until the next education session. Growth monitoring session will also be conducted in each session, whereby mothers will be taught and trained to weigh their children. |
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No Intervention: Comparison group
The comparison group will not receive any intervention but will be provided with the developed educational materials used in the program after the program has been completed.
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- Changes in body weight after 3 months of intervention in children [ Time Frame: 3 months ]body weight in kg
- Changes in weight-for-age z score after 3 months of intervention in children [ Time Frame: 3 months ]weight-for-age z score in standard deviation
- Changes in height-for-age z score after 3 months of intervention in children [ Time Frame: 3 months ]height-for-age z score in standard deviation
- Changes in weight-for-height z score after 3 months of intervention in children [ Time Frame: 3 months ]weight-for-height z score in standard deviation
- Changes in dietary intake after 3 months of intervention in children [ Time Frame: 3 months ]24-hour diet recall (3 days) in kcal
- Changes in diet quality after 3 months of intervention in children [ Time Frame: 3 months ]Healthy Eating Index (HEI) for Malaysians; composite HEI scores range from 0 to 100%; score <51% indicates poor diet quality, 51 to 80% indicates diet required improvement, and >80% indicates good diet quality
- Changes in nutrition knowledge after 3 months of intervention in mothers [ Time Frame: 3 months ]20-item nutrition knowledge questionnaire; total scores range from 0 to 20 marks; higher score indicates good knowledge
- Assessment of food security level after 3 months of intervention in mothers [ Time Frame: 3 months ]6-item USDA Short Form Food Security Survey Module; It consists of affirmative responses such as 'always', 'sometimes', and 'yes', as well as non-affirmative responses such as 'never', 'no', and 'don't know'. An affirmative response is given a score of 1 and a non-affirmative response is given a 0 score. The possible total scores range from 0 to 6, and a score of 2 or higher indicates food insecurity
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| Ages Eligible for Study: | 3 Years to 5 Years (Child) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
For Phase 1:
Inclusion Criteria:
- Malaysian
- Children aged 3 to 5 years old
- Mothers aged above 18 years old
- Living in public low-cost PPR flat
Exclusion Criteria:
- Children who are taken care by other adults rather than mothers such as father, grandparents and caregivers
- Mothers with mental disabilities
- Children with history of chronic diseases including congenital heart disease, liver disease, renal failure or sickle cell disease and any congenital abnormalities
- Children who are under treatment for communicable disease such as measles and chickenpox
- Children with learning disabilities
- Mother-child dyads involved in any other intervention or clinical research
- Children who are overweight or obese
The respondents' selection criteria in Phase 2 are almost similar as in Phase 1 except for the second inclusion criterion that is related to children. In Phase 2, only undernourished children (either underweight, stunting or wasting) aged 3 to 5 years old will be recruited in order to evaluate the effectiveness of the intervention in this particular group. The exclusion criteria in Phase 2 are similar to the exclusion criteria in Phase 1.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04688515
| Contact: Lok Poh Chek, PhDCandidate | +60165243872 | lokpoh95@yahoo.com |
| Principal Investigator: | Wan Ying Gan, PhD | Universiti Putra Malaysia |
| Responsible Party: | Gan Wan Ying, Associate Professor, Universiti Putra Malaysia |
| ClinicalTrials.gov Identifier: | NCT04688515 |
| Other Study ID Numbers: |
JKEUPM-2020-349 |
| First Posted: | December 30, 2020 Key Record Dates |
| Last Update Posted: | September 29, 2021 |
| Last Verified: | September 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Child undernutrition Positive deviance Urban poor children |
Stunting Wasting Weight gain |
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Malnutrition Child Nutrition Disorders Nutrition Disorders |

