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High Risk PregnancyNCT06279559

Music Therapy and High-risk Pregnancy

A study testing Music-therapy in people with High Risk Pregnancy, run by Istituto Giannina Gaslini at 1 site in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The objective of this clinical trial is to assess the impact of a music therapy intervention on reactive psychological components related to the risk of preterm birth in hospitalized pregnant women. The primary inquiries it seeks to address are: 1. Read more about this study

Who is it for?
Ages 18 years and older, women onlyHealthy volunteers can take part
Conditions the study is for
High Risk Pregnancy
What is being tested?
Music-therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
72 participants
Where
1 siteItaly
Study dates
1 Jun 2023to 1 Dec 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age over 18 years old
  • Adequate knowledge of the Italian language
  • Consent to participate
  • Condition of risk of preterm birth
  • Age over 18 years old
  • Adequate knowledge of the Italian language
  • Consent to participate

Who cannot join

  • Positive history of mental retardation
  • Difficulty understanding the Italian language
  • Presence of diagnosis of psychiatric pathology
  • Absence of informed consent
  • Positive history of mental retardation
  • Difficulty understanding the Italian language
  • Presence of diagnosis of psychiatric pathology
  • Absence of informed consent

Trial locations and contacts

1 site in 1 country.

Italy1 site, 1 recruiting
  • Istituto Giannina Gaslini

    Genova, 16147

    Cristina Venturino, 010 5636.2346, cristinaventurino@gaslini.org

    Recruiting

Other trials in Italy

About this study

Official title: Evaluating the Impact of Music Therapy on Psychological Well-being During High-risk Pregnancy

The objective of this clinical trial is to assess the impact of a music therapy intervention on reactive psychological components related to the risk of preterm birth in hospitalized pregnant women. The primary inquiries it seeks to address are:

  1. Can a music therapy intervention during high-risk pregnancy mitigate reactive psychological components (perceived emotional state, state anxiety and trait anxiety, depressive symptoms, perceived stress) related to the risk of preterm birth in hospitalized pregnant women?
  2. Does music therapy intervention during high-risk pregnancy positively influence the development of the attachment bond between the mother and the child?
  3. How does the risk of preterm birth modulate the future attachment bond between mother and child?
Read more

Participants will be categorized into three groups: a clinical experimental group (pregnant women at risk of preterm birth undergoing music therapy intervention), a clinical control group (pregnant women at risk of preterm birth receiving standard ward care), and a non-clinical control group (pregnant women with a physiologically progressing pregnancy).

Upon signing the informed consent, all three groups will be required to complete five self-report questionnaires assessing perceived positive and negative feelings, depressive symptoms, state anxiety and trait anxiety, perceived stress, and the mother-fetus attachment bond. Subsequently, the clinical experimental group will undergo ten online music therapy sessions, while the clinical control group will receive routine ward care. Following the music therapy sessions, both clinical groups will reassess the aforementioned measures. The non-clinical control group will complete the same self-report questionnaires with the same timing as the clinical groups. All three groups will be contacted three months after childbirth to complete a self-report questionnaire evaluating the postnatal attachment bond.

Researchers will compare the outcomes of the two clinical groups to address the first two research questions, while the comparison between the clinical control group and the non-clinical control group outcomes will be employed to answer the third research question.

Read the detailed description

Background and Rationale Every year, approximately 15 million children are born prematurely worldwide, with a global incidence of around 11%. Preterm birth occurs when labor takes place between the 22nd and 37th completed weeks of gestation, representing a significant public health concern. Preterm birth is associated with higher rates of infant morbidity and mortality, increased risk of long-term medical complications, impaired neurological development, family stress, and substantial social costs. Conversely, the risk of preterm birth is a stressful event for caregivers, particularly for pregnant women, potentially evolving into a traumatic experience, eliciting feelings of anxiety and depression. In cases of preterm birth risk, the initial phase of parenthood is marked by uncertainty, dominated by prevalent emotional correlates of anxiety and fear of death, which, in turn, diminish the psychological investment in the child. Many parents respond to this reality with an initial phase of rejection and ambivalence towards the child, expressing both frustration and common concerns about the infant's survival.

The risk of preterm birth falls under high-risk pregnancies, defined as "[...] any unexpected or unforeseen medical or obstetric condition associated with pregnancy with an actual or potential risk to the health or well-being of the mother or fetus...". Compared to women with low-risk pregnancies, those with high-risk pregnancies exhibit significantly higher levels of stress and anxiety, report more negative emotions when facing stress, and have a worse emotional state. Additionally, women confined due to high-risk pregnancies show predominant emotional responses of fear, anxiety, and emotional distance from the child, along with depressive symptoms and feelings of loneliness. Thus, the emotional impact of the risk of preterm birth on pregnant women demands adequate clinical attention, particularly considering that the reactive symptoms mentioned above serve as predictive factors when exploring the psychosocial determinants of preterm birth.

Furthermore, the risk of preterm birth can negatively influence the development of the mother-fetus attachment bond (or prenatal attachment), although some studies report contrasting results. Prenatal attachment, derived from John Bowlby's Attachment Theory, is defined as "the emotional bond that normally develops between the pregnant parent and their unborn child". It serves as an early indicator of the future quality of the mother-child attachment bond and is a crucial factor influencing the child's subsequent well-being. Women with high-risk pregnancies may experience guilt for their condition, and the risk of preterm birth and premature rupture of membranes can interrupt the psychological preparation process for motherhood. Negative thoughts in pregnant women related to fetal health and the possibility of fetal death can evoke fear of developing a relationship with the fetus, hindering attachment development.

Therefore, it becomes crucial to identify effective, non-invasive, and adaptable methods within the hospital setting to reduce unpleasant emotional states in pregnant women at risk of preterm birth and promote the structuring of the attachment bond. In this context, recent research has increasingly focused on music therapy as one of the potential approaches to alleviate emotional states linked to pregnancy.

The World Federation of Music Therapy defines music therapy as "[...] the professional use of music and its elements as an intervention in medical, educational, and social environments with individuals, groups, families, or communities seeking to optimize their quality of life and improve physical, social, communicative, emotional, intellectual, and spiritual health". Recent literature reviews and meta-analytical studies have documented how music therapy can be effective in reducing stress-related symptoms (both in medical and mental health contexts), decreasing depressive symptoms, and anxious symptoms. Regarding its use during pregnancy, music therapy, besides significantly reducing mental health problems such as anxiety, depressive symptoms, and perceived stress in pregnant women, can address the sensory, physical, and emotional needs of pregnant women and support the process of creating the attachment bond, promoting the development of meaningful interactions.

In conclusion, the risk of preterm birth requires prolonged hospitalization for pregnant women. It can have a high impact on both individual and couple's emotional and psychological well-being, as well as on the construction of the mother-child relationship. Hospitalization, while serving as a protective element and monitoring for the health of the unborn, intensifies fears and anxieties, inducing a "medicalization" that may be accompanied by feelings of inadequacy and helplessness. This, coupled with concerns about the effects of gestational complications on the fetus, can negatively influence the adaptation process to pregnancy and the development of the mother-child attachment. However, although numerous studies have delved into the topic of prenatal mother-child attachment development in normal pregnancies, the development of this relationship in high-risk pregnancies remains understudied. Additionally, to the best of our knowledge, the potential benefit of music therapy on the mental health of women with high-risk pregnancies and on pre- and post-natal attachment bonding is still underexplored in the literature of the field.

STUDY OBJECTIVES - Primary Objectives: The primary aim is to evaluate the effect of a music therapy intervention on reactive psychological components associated with the risk of preterm birth in hospitalized pregnant women.

The key psychological components of interest in this study include depressive symptoms, anxious symptoms, perceived stress, perceived well-being, prenatal attachment, and postnatal attachment.

  • Secondary Objectives:

The secondary objectives are as follows:

  1. - Assessment of Attachment Quality: To assess whether there are variations in the quality of pre-and postnatal attachment in hospitalized pregnant women at risk of preterm birth who do not undergo music therapy compared to pregnant women with uncomplicated pregnancies.
  2. - Psychosocial Well-being: To identify aspects of psychosocial well-being influenced by music therapy intervention and those that do not appear to be affected.
  3. - Timing of Intervention: To investigate whether differences in the gestational age at which music therapy intervention is conducted play a significant role in treatment efficacy.
  4. - Pregnancy Characteristics and Personal History: To explore whether different aspects of the current pregnancy and the pregnant woman's personal, pathological, and physiological history, encompassing both behavioural and emotional factors, influence the effectiveness of the treatment.
  5. - Demographic Variables: To examine whether sociodemographic variables influence the outcomes of music therapy intervention.

STUDY SETTING AND EXPERIMENTAL PHASES

Setting and Participant Recruitment:

To assess the effectiveness of the music therapy intervention, all consecutively hospitalized patients with a high risk of preterm birth at the Obstetrics and Gynecology Unit of I.R.C.C.S. Giannina Gaslini will be enrolled. They will be randomly assigned to either the experimental or control group. Additionally, to examine the impact of the preterm birth risk on the formation of attachment bonds, pregnant women with uncomplicated pregnancies attending check-ups at the same unit will be consecutively recruited. The sample will be recruited based on predefined inclusion criteria. Once invited to participate and after obtaining consent, patients will be recruited for the study.

Administration and Recruitment Phases:

The test administration phases will take place in the inpatient rooms of the Obstetrics and Gynecology Unit, in a protected setting, and/or through telecommunication methods. Music therapy interventions will be conducted exclusively via telecommunication.

  1. st Phase: Patients will be asked for authorization to participate in the study. A detailed explanation of the study procedures, structured and identical across participants, will be provided to avoid influencing test completion or participant behaviour. The experimenter will ask patients to read and sign the study information sheet, informed consent form, and data processing consent. A patient will be considered enrolled only after obtaining authorization.
  2. nd Phase: In the second phase, all participants will be asked to complete a form for collecting demographic and medical data along with six self-report questionnaires assessing perceived subjective well-being (PANAS), characteristics of mother-fetus attachment or prenatal attachment (MAAS), perceived stress levels (PSS), mood deflection and depressive symptoms (EPDS), and state and trait anxiety components (STAI-Y).
  3. rd Phase: The third phase involves the music therapy intervention, exclusively for participants assigned to the clinical experimental group. Specifically, participants in the clinical experimental group will undergo a series of 10 music therapy sessions conducted by Dr. Francesca Pasini and Dr. Alessandra Ravizza. These sessions will be conducted via telecommunication and will have a high degree of structure in terms of both the course and content. Conversely, all other participants will receive standard ward care.
  4. th Phase: Within one week after the conclusion of the music therapy intervention (to which only the experimental clinical group will be subjected), all participants will be asked to complete the self-report questionnaires administered during the 2nd phase again.
  5. th Phase: All the participants will be contacted via email for a follow-up to assess the characteristics of mother-infant attachment or postnatal attachment (MPAS) three months after childbirth.

Timeline:

The duration of the two data collection sessions (pre and post-treatment) will mirror that of the standard session (approximately 50 minutes) as measurements will be taken during clinical hours. Each music therapy session will last approximately 75 minutes. It is noteworthy that the number of music therapy sessions will depend on the patient's therapeutic progress, availability, and treatment timing at the enrollment date.

Being tested
Music-therapy
Keywords
music-therapy, high-risk pregnancy, attachment bond

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Music-therapyBehavioural

    10 sessions of online music therapy held by expert music therapists

Study groups in NCT06279559
Study groupRoleWhat they receive
clinical experimental groupExperimentalpregnant women with the risk of preterm birth who will undergo music therapy intervention
Receives: Behavioral: Music-therapy
clinical control group and non-clinical control groupNo interventionpregnant women with the risk of preterm birth who will receive the usual ward care and pregnant women with pregnancy with a physiological course

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Depressive symptoms

    Edimburg Prenatal Depression Scale (EPDS)

    Measured: administered before and within one week after the conclusion of the music therapy intervention

  2. State anxiety and trait anxiety

    State-Trait Anxiety Inventory - Forma Y (STAI-Y)

    Measured: administered before and within one week after the conclusion of the music therapy intervention

  3. Perceived stress

    Perceived Stress Scale (PSS)

    Measured: administered before and within one week after the conclusion of the music therapy intervention

  4. Perceived positive and negative feelings

    Positive and Negative affect Schedule (PANAS)

    Measured: administered before and within one week after the conclusion of the music therapy intervention

  5. Mother-fetus attachment bond

    Maternal Antenatal Attachment Scale (MAAS)

    Measured: administered before and within one week after the conclusion of the music therapy intervention

  6. Mother-child attachment bond

    Postpartum Attachment Scale (MPAS)

    Measured: administered three months after the childbirth

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Feb 2024
  2. Study start1 Jun 2023
  3. Primary completion1 Dec 2024 (estimated)
  4. Study completion1 Dec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
72 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06279559
Sponsor's protocol ID
MTinHRP_v1_10/01/2023
Status last verified
Feb 2024
First submitted
14 Feb 2024
Last updated
28 Feb 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Music-therapy in people with High Risk Pregnancy, run by Istituto Giannina Gaslini at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 28 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Cristina Venturino (010 5636.2346, cristinaventurino@gaslini.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Depressive symptoms (time frame: administered before and within one week after the conclusion of the music therapy intervention). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Feb 2024.

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