Personalized Mobile Pregnancy Program (PMPP): development and evaluation.

Personalized Mobile Pregnancy Program (PMPP): development and evaluation. - Personal Mobile Pregnancy Programme (PMPP).

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON31953

Enrollment

538

Registered

2008-10-03

Start date

2008-05-01

Completion date

Unknown

Last updated

2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

zwangerschapscomplicaties en ziekten tgv roken en of alcoholgebruik pregnancy complications

Interventions

PMPP: Intervention on the lifestyle factors (folic acid, vegetables, fruits, alcohol, smoking) is based on (mobile) internet and SMS

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Dutch language in word, reading and understanding pregnancy wish alcohol use smoking

Exclusion criteria

Exclusion criteria: Not familiar with the Dutch language no pregnancy wish

Design outcomes

Primary

Measure	Time frame
Study A -Content evaluation. The content evaluation consists of the following: opinions on the number and length of the questions and messages, (technical) usability, readability, comprehensibility, attractiveness and convenience and ease of navigating through the PMPP, perceived personal relevance, individualization, accuracy and persuasiveness of the feedback. A debriefing interview with each woman to gain additional information about usability, applicability and acceptance will be held. - Process evaluation: Type of mobile phone, for what services they use their mobile phone (e.g. calling, SMS, WAP, MMS), frequency of use of these services are measures of feasibility (% of a sample owning a mobile phone and using specific mobile phone services) and acceptance (% of those owning a mobile phone and agreed to provide their mobile phone number to participate). Server registrations of the number of sent and returned questions and messages and the speed of response delivers quantitative information on usability and applicability. Outcome measures of process and content are compared for different groups of participants (e.g. socio-economic status, ethnic groups). Study B - short term primary outcome: proportion of women who smoke, the proportion of women who use alcohol, as measured at 1 and 6 months after the start of the intervention - long term primary outcome: proportion of women who smoke, the proportion of women who use alcohol, as measured at +13 months and +18 months after the start of the intervention (= +1 month and +6 months after the PMPP-interventions has ended).	—

Measure

Time frame

Study A -Content evaluation. The content evaluation consists of the following: opinions on the number and length of the questions and messages, (technical) usability, readability, comprehensibility, attractiveness and convenience and ease of navigating through the PMPP, perceived personal relevance, individualization, accuracy and persuasiveness of the feedback. A debriefing interview with each woman to gain additional information about usability, applicability and acceptance will be held. - Process evaluation: Type of mobile phone, for what services they use their mobile phone (e.g. calling, SMS, WAP, MMS), frequency of use of these services are measures of feasibility (% of a sample owning a mobile phone and using specific mobile phone services) and acceptance (% of those owning a mobile phone and agreed to provide their mobile phone number to participate). Server registrations of the number of sent and returned questions and messages and the speed of response delivers quantitative information on usability and applicability. Outcome measures of process and content are compared for different groups of participants (e.g. socio-economic status, ethnic groups). Study B - short term primary outcome: proportion of women who smoke, the proportion of women who use alcohol, as measured at 1 and 6 months after the start of the intervention - long term primary outcome: proportion of women who smoke, the proportion of women who use alcohol, as measured at +13 months and +18 months after the start of the intervention (= +1 month and +6 months after the PMPP-interventions has ended).

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Secondary

Measure	Time frame
Study B (1) if case of no cessation: the amount of reduction in smoking and/or a reduction in alcohol use; (2) outcomes of biomedical measurements and blood sampling; both assessed at baseline, +1, +6, +13 and +18 months after start of the intervention. For analytical purposes, participants who both smoke and use alcohol are considered a primary success if at least one of these risk factors is stopped. Differential effects according to the interventions on smoking and/or alcohol in the same person, pregnancy, ethnicity, and SES will be further explored.	—

Measure

Time frame

Study B (1) if case of no cessation: the amount of reduction in smoking and/or a reduction in alcohol use; (2) outcomes of biomedical measurements and blood sampling; both assessed at baseline, +1, +6, +13 and +18 months after start of the intervention. For analytical purposes, participants who both smoke and use alcohol are considered a primary success if at least one of these risk factors is stopped. Differential effects according to the interventions on smoking and/or alcohol in the same person, pregnancy, ethnicity, and SES will be further explored.

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Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)