Effectiveness of mHealth Education on Health Outcomes Among Pregnant Women

Pregnant Women Clinical Trial

Official title:

A Dietitian-led Cluster Randomised Controlled Trial on the Effectiveness of mHealth Education on Health Outcomes Among Pregnant Women

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05377151
• Other study ID #: 03210224
• Status: Recruiting
• Phase: N/A
• Start date: April 1, 2023
• Est. completion date: June 30, 2024

Study information

• Verified date: September 2023
• Source: Universiti Putra Malaysia
• Contact: Yoke Mun Chan
• Phone: 03-97692433
• Email: cym[@]upm.edu.my
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Gestational weight gain (GWG), weight gain of a mother during pregnancy, is an important determinant that influence the health outcomes of mothers and fetus. There is an increasing trend of pregnant women using mobile health (mHealth) to assess for pregnancy-related health information. While evidence on the effectiveness of mHealth education on improving pregnancy outcomes among pregnant women is growing, the findings had been inconclusive with scarcity of such data in Malaysia. The objective of the study is to determine the effectiveness of a 9-month mHealth intervention on GWG and other outcomes (prenatal knowledge, physical activity, psychosocial well-being, nutritional status, quality of life and sleep quality) among pregnant women.

Description:

This study will evaluate the usability, feasibility and practicality of a previously developed smartphone application with complete alpha and beta testing on pregnancy outcomes in a cluster randomised control trial (RCT). The study will be completed by involving the nutrition intervention using either mHealth interventions or conventional methods that will be carried out among pregnancy women. Subjects will be allocated into groups according to respective health clinics, namely, two interventions group which are: Group 1: mHealth intervention group Group 2: mHealth intervention group + dietitian consultation Group 3: control group which total of 294 eligible subjects will be recruited, with 98 subjects are needed in respective groups. This is a cluster-randomised controlled trial. For Malaysia consist of two regions which are East Malaysia and West (or peninsular) Malaysia and they are actually about 400 miles (640 km) apart. At East Malaysia, we targeted on the area with higher density of population which are Klang Valley (Kuala Lumpur, Selangor and Putrajaya). As shown in Figure 1, for three states under Klang Valley, we obtained ethics approval from the Jabatan Kesihatan Negeri Selangor for Selangor state and Jabatan Kesihatan Wilayah Persekutuan Kuala Lumpur dan Putrajaya for Putrajaya state. In order to prevent cross contamination between the states, we use simple random sampling which Selangor been allocated into control group and Putrajaya as intervention group. As under Putrajaya states only two clinics granted approval for data collection which are Presint 9 Health Clinic and Presint 18 Health Clinic. By using cluster sampling method, Presint 9 Health Clinic was randomised into intervention group 1 which whole cluster participant will be receiving mHealth intervention alone and Presint 18 Health Clinic into intervention group 2 which whole cluster participants will receive mHealth intervention group in addition with personal dietitian consultation. There are nine districts in Selangor: Gombak, Hulu Langat, Hulu Selangor, Klang, Kuala Langat, Kuala Selangor, Petaling, Sabak Bernam and Sepang which consist of total of 81 health clinics, we stratified the number of health clinics within the 25 km radius from the Faculty of Medicine and Health Sciences, Universiti Putra Malaysia due to the geographical proximity and financial constraints (limited budget). There were total of 15 health clinics after stratification and simple random sampling was done which Seri Kembangan health clinics in Petaling District had been chosen as control group. As this is an intervention study, thus blinding is not applicable for data collection personnel and participants. The health clinics that involved in this study will be maternal and child health clinics. This study will use a set of questionnaires to obtain information on personal information, anthropometry data, prenatal knowledge, physical activity, psychosocial well-being, dietary intake, quality of life, sleep quality and gestational weight gain of the subjects, based on appropriate instruments. Re-assessment will be performed at month-6 and month-9 (delivery) after baseline measurements. During the re-assessment, the data will be collected again on dietary intake, physical activity, psychosocial well-being, sleep quality and quality of life. All subjects will be followed up prospectively until delivery. The follow up data collection will be matched with the prenatal visit of the pregnant mother to the clinic.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 294
• Est. completion date: June 30, 2024
• Est. primary completion date: September 30, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Malaysian women
• 18 - 40 years old
• Single pregnancy
• At first trimester or second trimester
• All ethnicities
• Meet or did not meet with dietitian before
• With or without diseases (diabetes mellitus with/ without low dose insulin, hypertension, hyperlipidaemia, overweight/ obese)
• Own smart phone with internet access
• All BMI categories

Exclusion Criteria:

• Diagnosed by medical doctor with major psychiatric problems (bipolar depression, schizophrenia, suicidal risk)
• Multiple pregnancies
• On other intervention program
• Grand multipara
• Severe comorbidities (cardiac diseases, severe anaemia)
• Type 1 diabetes mellitus or Type 2 diabetes mellitus with high dose insulin

Related Conditions & MeSH terms

• Pregnant Women

Intervention

Other:
• Mobile application
Nutrition intervention using either mHealth interventions or conventional methods will be carried out among pregnant women). Subjects will be allocated into three groups, namely, two interventions group which are: Group 1: mHealth intervention group (98 subjects) Group 2: mHealth intervention group + dietitian consultation (98 subjects) Group 3: control group (98 subjects)

Locations

Country	Name	City	State
Malaysia	Presint 18 Health Clinic	Putrajaya
Malaysia	Presint 9 Health Clinic	Putrajaya
Malaysia	Seri Kembangan Health Clinic	Seri Kembangan	Selangor

Sponsors (1)

Lead Sponsor	Collaborator
Universiti Putra Malaysia

Country where clinical trial is conducted

Malaysia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in Gestational Weight Gain	Weight gain (kg)	3 points time (Baseline, 6th month, 9th month/ delivery)
Secondary	Prenatal knowledge	The maternal health literacy inventory in pregnancy (MHELIP); MHELIP score to 4 categories: 'inadequate', 'problematic' (which together also define 'limited' health literacy), 'sufficient and 'excellent' (which together also defined 'desired' health literacy): Inadequate= 0-50 Problematic= 50.1-66 Sufficient= 66.1-84 Excellent=84.1-100	1 point1 time (Baseline)
Secondary	Physical activity	Pregnancy Physical Activity Questionnaire (PPAQ); The activity was classified by intensity: sedentary (< 1.5 METs), light (1.5- < 3.0 METs), moderate (3.0-6.0 METs) or vigorous (> 6.0 METs) and the average number of MET-hours per week expended in each intensity level was calculated. The higher the score, the more active the subject is.	2 points time (Baseline, 6th month)
Secondary	Psychosocial well-being	Depression Anxiety and Stress Scale (DASS-21); Scores on the DASS-21 will need to be multiplied by 2 to calculate the final score.; Depression (Normal: 0-9; Mild: 10-13; Moderate: 14-20; Severe: 21-27; Extremely Severe: 28+) Anxiety (Normal: 0-7; Mild: 8-9; Moderate: 10-14; Severe: 15-19; Extremely Severe: 20+) Stress (Normal: 0-14; Mild: 15-18; Moderate: 19-25; Severe: 26-33; Extremely Severe: 34+)	3 points time (Baseline, 6th month, 9th month/ delivery)
Secondary	Nutritional status	24-hour dietary recall (2 weekdays and 1 weekend)	3 points time (Baseline, 6th month, 9th month/ delivery)
Secondary	Quality of life (well being)	WHO 5 item well being index; The raw score is calculated by totalling the figures of the five answers. The raw score ranges from 0 to 25, 0 representing worst possible and 25 representing best possible quality of life.; To obtain a percentage score ranging from 0 to 100, the raw score is multiplied by 4. A percentage score of 0 represents worst possible, whereas a score of 100 represents best possible quality of life.	3 points time (Baseline, 6th month, 9th month/ delivery)
Secondary	Sleep quality	Pittsburgh Sleep Quality Index (PSQI); In scoring the PSQI, seven component scores are derived, each scored 0 (no difficulty) to 3 (severe difficulty). The component scores are summed to produce a global score (range 0 to 21). Higher scores indicate worse sleep quality.	3 points time (Baseline, 6th month, 9th month/ delivery)
Secondary	Pregnancy outcome (Type of delivery)	Spontaneous vaginal delivery (SVD): Cephalic/ Breech/ Assisted Breech; Instrumental Delivery: Forceps/ Vacuum; Caesarean: Elective/ Emergency/ Lower segment Caesarean section (LSCS)/ Classical	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Apgar Score)	@1 minute and @5 minutes (Apgar Score 7-10: Good outcome)	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Born term)	Yes / No (_______ week)	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Infant weight)	weight (kg)	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Infant length)	length (cm)	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Infant head circumference)	head circumference (cm)	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome ( Infant breast circumference)	breast circumference (cm)	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Infant gender)	Male/ Female	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Maternal complications)	Postpartum hemorrhage (PPH)/ Eklampsia / Retained placenta/ Venous thromboembolism (VTE)/ Postpartum depression	1 point time (9th month/ delivery)
Secondary	Pregnancy outcome (Infant complications)	Miscarriage/ Prematurity/ Stillbirth/ Congenital anomalies/ Shoulder dystosia/ Jaundice / Respiratory related / Transient Tacypnoiec of newborn (TTN)/ Pneumonia (lung infection)	1 point time (9th month/ delivery)