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The effect of premature infant oral motor intervention by the mother on mothers' mood

Effectiveness of Premature Infant Oromotor Intervention by mother on the situation of mood in mothers of premature infants

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230423057977N1
Enrollment
74
Registered
2023-06-20
Start date
2023-06-22
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Mood.

Interventions

Intervention 1: Intervention group: The mood questionnaire will be filled in at the beginning of the study by the mother, who both herself and her baby meet the inclusion criteria. And oral motor inte

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: For mothers, entry conditions include: no history of infertility Uncomplicated pregnancy Desire to be pregnant No history of physical and mental illness No addiction Lack of accidents during the last three months (according to the participant) The conditions for the inclusion of infants in the study include: 1) infants with a gestational age of 29-34 weeks, 2) having physiological stability and no stress symptoms at the time of stimulation, 3) without cleft palate, cleft lip, and temperament abnormalities, 4) infants with an Apgar score of 5 or more than 7

Exclusion criteria

Exclusion criteria: Mother's unwillingness to continue participating in the study Early discharge of the baby with the personal consent of the parents Transferring the baby to another treatment center Not having the ability to intervene Incompleteness of 20% of the completed information of the forms The conditions for the exclusion of infants from the study: 1) sepsis 2) heart disease 3) necrotizing enterocolitis 4) grade 3 and 4 intraventricular hemorrhage (according to sonography that is routinely performed in the first week) 5) severe asphyxia

Design outcomes

Primary

MeasureTime frame
Mood score in POMS standard questionnaire. Timepoint: Measuring the mood score at the beginning of the study (before the intervention) and 10 days after the intervention. Method of measurement: Standard Mood Questionnaire (POMS).

Secondary

MeasureTime frame
Participation. Timepoint: The questionnaire will be filled at the beginning of the study and 10 days later. Method of measurement: Questionnaire POMS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Hosseinzadeh

Tehran University of Medical Sciences

sahar.hosseinzadeh@ymail.com+98 21 4223 5503

Outcome results

None listed

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