Efficacy and Feasibility of an eHealth Intervention for Pregnant Women on Diet, Physical Activity and Knowledge Related to Pregnancy
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- University of Oviedo
- Enrollment
- 153
- Locations
- 1
- Primary Endpoint
- Following physical activity recommendations (mean)
Study Overview
Brief Summary
A pragmatic clinical trial are developed with the aim to assess the effectiveness and feasibility of using an app as complement of the usual care that receive pregnancy women in a sanitary area in the Principado de Asturias (Spain).
Participants are pregnancy women attended in the sanitary area number 3 of the Pincipado de Asturias. As inclusion criteria we will consider: i) aged over 18; ii) pregnant with only 1 fetus; iii) low risk pregnancy; iv) smartphone Access; v) signed the informed consent. As exclusion criteria: i) non-fluent Spanish speaker; ii) do not fill the questionnaires.
A randon sample of 153 women will be recruited consequtively, at the first triemester, from the midwife consulting room. Those women to agreed to participate, and sign the infomred consent, will be anonymizated using a alphanumerical code and asigned (according to a previous randomization distribution by code) to a control or an intervention group.
All women are going to receive the baseline and post intervention questionnaires by email. All women are going to receive the usual care. Adittionally, those in the intervention group, will be prompted to use iNATAL app.
The following questionnaires and measures will be used: uMARS Questionnaire to assess and percentage of app usage tot assess the feasibility; to assess the effectiveness: Motiva.Diaf to assess dietary and physical activity recommendations; ad hoc questionnaire to assess knwoldedge pregnancy related; mother complications during of after the pregnancy period and newborn complications.
The intervention takes all pregnancy period.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •aged over 18
- •pregnant with only 1 fetus
- •low risk pregnancy
- •smartphone Access
- •signed the informed consent
Exclusion Criteria
- •non-fluent Spanish speaker
- •do not fill the baseline or post-intervention questionnaires
Arms & Interventions
Control group
- Sign consent form and baseline assessments
- Usual care
- Post intervention assessments
Interention group
- Sign consent form and baseline assessments
- Usual care + app iNATAL
- Post intervention assessments
Intervention: App intervention (Behavioral)
Outcomes
Primary Outcomes
Following physical activity recommendations (mean)
Time Frame: Change from Baseline dietary recommendations at 8 or 9 months (depending the pregnancy)
For both groups. Compliance with dietary recommendations. We are going to use the Motiva.Diaf questionnaire. It includes 5 questions to assess healthy diatery adherence. Response in dichotomous option 0 (not follow the recommendation) or 1 (follow the recommendation). Total score range from 0 (null dietary compliance) to 5 (best dietary compliance).
Following dietary recommendations (mean)
Time Frame: Change from Baseline dietary recommendations at 8 or 9 months (depending the pregnancy)
For both groups. Compliance with dietary recommendations. We are going to use the Motiva.Diaf questionnaire. It includes 7 questions to assess healthy diatery adherence. Response in dichotomous option 0 (not follow the recommendation) or 1 (follow the recommendation). Total score range from 0 (null dietary compliance) to 7 (best dietary compliance).
Change in pregnancy knwoledge (mean)
Time Frame: Change from Baseline dietary recommendations at 8 or 9 months (depending the pregnancy)
For both groups. Ad hoc questionnaire that includes 10 questions related with pregnancy care. Response in dichotomous option 0 (wrong answer) or 1 (correct answer). Total score range from 0 (null knowledge) to 7 (best knowledge).
Newborn complications (mean)
Time Frame: From birth to one week after.
Number of complication suffer by the newborn in the first week after the birth.
App ussage
Time Frame: At the end of the intervention (8-9 after baseline)
Only for intervention group. Use the app during pregnancy period time. Dichotomous answer (yes or not).
App quality (mean)
Time Frame: At the end of the intervention (8-9 after baseline)
Only for intervention group. We are going to use the Spanish version of uMARS to assess the objective and subjetive quality of the app. Both dimensions has a total score range from 1 (lowest quality) to 5 (higher quality).
Women weigh gain (mean)
Time Frame: From baseline to the end of the intervention (8-9 months after baseline)
Weigh improvement in kilograms during the pregnancy period time
Secondary Outcomes
No secondary outcomes reported
Investigators
Rubén Martín Payo
Associate professor
University of Oviedo