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A trial exploring the feasibility of using telephone support (SMS and call) as a means of supporting young mothers (12-19 years) in Western Kenya soon after giving birth

A pilot randomised controlled trial to explore Telephone Support Intervention as a means of supporting young mothers in the immediate postnatal period in Western Kenya

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15017499
Enrollment
50
Registered
2017-07-17
Start date
2017-05-11
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Midwifery care - postnatal care of young mothers Pregnancy and Childbirth Midwifery care - postnatal care of young mothers

Interventions

This pilot study seeks to assess the feasibility and acceptability of telephone support intervention in the postnatal care of young mothers. The sample size follows accepted guidelines for feasibility
and a call) among young mothers (12-19 years) in western Kenya. The study participants are recruited and randomised to either the intervention or control groups during the first week postpartum (befor

Sponsors

University of Mancester
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. All young postnatal mothers aged 12-19 years who have given birth to a singleton healthy baby at term at the respective centres (MTRH and KCRH) 2. Those for whom consent has been sought and/or those whose parents/guardians consent, and willing to participate in the study 3. Postnatal young mothers who own a mobile phone and are able to use common mobile telephone operation services 4. Ability to read telephone text to a basic level of understanding 5. Qualified midwives and/or nurse-midwives with more than one year experience working in maternity setting

Exclusion criteria

Exclusion criteria: 1. Young postnatal mothers who have given birth through caesarean, or who had multiple pregnancies and/or whose babies developed birth complications or have congenital anomalies 2. Mothers who have no capacity to consent and/or participate (with severe mental disability/illness and/or learning disability. These groups of mothers will be excluded since they may require specific care due to their complex needs.

Design outcomes

Primary

MeasureTime frame
1. Feasibility and acceptability of the intervention is measured using reviews of the quality data available that supports a main trial and qualitative interviews at ten weeks for young mothers and 12 weeks for midwives 2. Quality of data available that support a main trial by reviewing patient notes/files at baseline

Secondary

MeasureTime frame
1. Maternal social support is measured using the maternal social support at ten weeks postpartum 2. Maternal self-esteem is measured using the Rosenberg Self-esteem scale at ten weeks postpartum 3. Mother infant bonding is measured using the postpartum bonding instrument at ten weeks postpartum 4. Postnatal depression is measured using the Edinburgh Postnatal depression scale at ten weeks postpartum

Countries

Kenya

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026