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A Randomized Controlled Trial of the Efficacy of the Lighthouse Parenting Programme in Addressing Parenting Difficulties in China

A Randomized Controlled Trial of the Efficacy of the Lighthouse Parenting Effectiveness Enhancement Programme in Addressing Parenting Difficulties

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06858059
Enrollment
68
Registered
2025-03-05
Start date
2025-04-04
Completion date
2026-05-20
Last updated
2026-07-07

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

Conditions

Parenting Intervention

Keywords

Parenting Intervention

Brief summary

The study will be conducted in three phases: assessments, group intervention and individual intervention. All participants will engage in the full program over a period of five weeks, divided into ten sessions. The 5 group interventions will occur once a week for 1.5 hours. During this time, the psychotherapist will disseminate psychological knowledge and skills pertinent to parenting, after which the group members will engage in practice exercises and discourse. Subsequently, one individual session will be conducted each week for one hour. The test group (Group A) will be assessed once at recruitment and after the last individual session. The control group (Group B) will undergo the same intervention as the test group after the test group completes the intervention and posttest, and will be assessed one additional time for pre-intervention status.

Interventions

OTHERpsychological intervention

All participants of the lighthouse parenting programme will engage in the full program over a period of five weeks, divided into ten sessions. The 5 group interventions will occur once a week for 1.5 hours. During this time, the psychotherapist will disseminate psychological knowledge and skills pertinent to parenting, after which the group members will engage in practice exercises and discourse. Subsequently, one individual session will be conducted each week for one hour.

Sponsors

Zhujiang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 70 Years
Healthy volunteers
No

Inclusion criteria

* Parents with children aged 2-14 years who exhibited parenting that were identified as being problematic (Parenting Stress Indicator PSI ≥ 86 (critical high level)).

Exclusion criteria

* Parents in the family with either parent and child who have a serious medical condition (e.g., cancer, heart disease, etc.), an acute psychotic episode, or difficulty engaging in group interventions may be excluded from participation.

Design outcomes

Primary

MeasureTime frameDescription
Parenting stressFrom enrollment to the end of treatment at 5 weeksThe Parenting Stress Index/Short Form (PSI/SF; Abidin, 1986) is employed to assess parenting stress.

Secondary

MeasureTime frameDescription
Parental mentalisingFrom enrollment to the end of treatment at 5 weeksThe Parental Reflective Functioning Questionnaire (PRFQ; Luyten, Mayes, Nijssens, \& Fonagy, 2017) is employed to assess parental mentalizing.
Quality of the parent-child relationshipFrom enrollment to the end of treatment at 5 weeksThe quality of the parent-child relationship is evaluated using the Multiperspective Parent-Child Relationship Questionnaire (M-PCR; Müller \& Achtergarde, 2018).
parenting efficacyFrom enrollment to the end of treatment at 5 weeksThe Brief Parental Self-Efficacy Scale (Woolgar et al., 2023) is employed to assess parenting efficacy.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 8, 2026