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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeUp to 70
SponsorZhujiang Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • psychological intervention

    Other 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.

Treatment groups

56 Participants
are divided into 2 treatment groups
Group A: The test group (Group A)Experimental treatment 1 intervention
Group B: The control group (Group B)No intervention 0 interventions

Trial outcomes

Primary outcomes

1

Parenting stress

The Parenting Stress Index/Short Form (PSI/SF; Abidin, 1986) is employed to assess parenting stress.

Time frame
From enrollment to the end of treatment at 5 weeks

Secondary outcomes

1

Parental mentalising

The Parental Reflective Functioning Questionnaire (PRFQ; Luyten, Mayes, Nijssens, \& Fonagy, 2017) is employed to assess parental mentalizing.

Time frame
From enrollment to the end of treatment at 5 weeks
2

Quality of the parent-child relationship

The quality of the parent-child relationship is evaluated using the Multiperspective Parent-Child Relationship Questionnaire (M-PCR; Müller \& Achtergarde, 2018).

Time frame
From enrollment to the end of treatment at 5 weeks
3

parenting efficacy

The Brief Parental Self-Efficacy Scale (Woolgar et al., 2023) is employed to assess parenting efficacy.

Time frame
From enrollment to the end of treatment at 5 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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