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ALAS PROPIAS: Music Therapy for Women Experiencing Machista Violence in Intimate Partner Relationships

NCT07925723, Not applicable, Active not recruiting, Universidad Miguel Hernandez de Elche

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleALAS PROPIAS: Music Therapy for Women Experiencing Machista Violence in Intimate Partner RelationshipsClinicalTrials.gov
NCT numberNCT07925723ClinicalTrials.gov
StatusActive not recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment67 participants, actualClinicalTrials.gov
Lead sponsorUniversidad Miguel Hernandez de ElcheClinicalTrials.gov
ConditionsIntimate Partner Violence (IPV), Intimate Partner Violence Against WomenClinicalTrials.gov
InterventionsExperimental Group (ALAS PROPIAS)ClinicalTrials.gov
First posted2026-11-09ClinicalTrials.gov
Last updated2026-11-09ClinicalTrials.gov

Registered outcomes 6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange in Self-EsteemBaseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)Change in self-esteem from pre-test to post-test, measured using the Rosenberg Self-Esteem Scale in both the experimental group and the wait-list control group.ClinicalTrials.gov
PrimaryChange in AnxietyBaseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)Change in anxiety from pre-test to post-test, measured using the State-Trait Anxiety Inventory (STAI) in both the experimental group and the wait-list control group.ClinicalTrials.gov
PrimaryChange in DepressionBaseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)Change in depression from pre-test to post-test, measured using the Beck Depression Inventory-II (BDI-II) in both the experimental group and the wait-list control group.ClinicalTrials.gov
PrimaryChange in Psychological Well-BeingBaseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)Change in psychological well-being from pre-test to post-test, measured using the Ryff Psychological Well-Being Scales in both the experimental group and the wait-list control group.ClinicalTrials.gov
PrimaryChange in Quality of LifeBaseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)Change in quality of life from pre-test to post-test, measured using the GENCAT Quality of Life Scale in both the experimental group and the wait-list control group.ClinicalTrials.gov
PrimaryChanges in Mood-Related Indicators During the Music Therapy InterventionAt the beginning and end of each of the 12 music therapy sessions for the SAM; at the end of each session for the researcher's observational recording tool.
Changes in mood-related indicators are assessed in the experimental group throughout the 12-session group active music therapy intervention. The researcher uses a structured observational recording tool to document indicators associated with six emotional states: sadness, anger, shame, insecurity, fear, and happiness. The indicators include participants' verbal expressions, facial expressions, posture, vocal characteristics, participation in musical activities, and interactions with other group members. In addition, participants complete the Self-Assessment Manikin (SAM) at the beginning and end of each session to assess their momentary affective responses
ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)