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Parent TrainingNCT06966323

Hold me Tight/Let me Go: Effectiveness of a Course to Enhance Parent-adolescent Relationship

An observational study of Parent Training and Parent Child Relationship, run by University of Amsterdam at 5 sites in Netherlands.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

HmT/LmG is a group course for 4-6 parental dyads and consists of 4 group sessions with psycho-education and skills training and 3 individual sessions per family (i.e., 1 session with the adolescent, 1 session with the parents, and 1 session with parents and adolescent together). Read more about this study

Who is it for?
Ages 12 to 18 years
What is being tested?
Hold me Tight / Let me Go
How many people
150 participants
Where
5 sitesNetherlands
Study dates
11 Jun 2025to 1 Sep 2028
Phase
Observational
Are there results?
Not yet: the study is under way

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 12 to 18 years
  • All sexes
  • Child, Adult

Study population: Families with adolescents aged 12 to 18 years will be recruited via participating clinical practices (mental health organizations) in the Netherlands. Recruitment will focus on families experiencing difficulties in the parent-adolescent relationship that are believed to contribute to the adolescent's emotional or behavioral problems. The population includes single-parent families, two-parent families, and blended families. The intervention is offered in the context of regular care.

We will include:

  1. Families with one or both parents/primary caretaker (single parent or blended families are allowed) with one adolescent of 12 to 18 years of age;
  2. Adolescent problems are deemed to be exacerbated by a stressful parent-adolescent relationship.

We will exclude:

  1. Participants in command of the Dutch language.
  2. Parents/primary caretakers and adolescents with severe psychopathology (e.g., psychosis, acute suicidality, severe depression) that will interfere with participation in the program.
  3. Parents/primary caretakers already attending systemic therapy or intensive parental guidance during the waiting period and during HmT/LmG. Other individual therapy will be registered during intake, and afterwards by the therapists. During follow-up systemic interventions are allowed but have to be registered.

Trial locations and contacts

5 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Sophie Jonker, Master of Science contact

31652365964

s.jonker@uva.nl

5 sites in 1 country

Netherlands5 sites, 3 recruiting
  • Connected Together

    Almere Stad

    Active, not recruiting
  • Molemann Mental Health

    Almere Stad

    Active, not recruiting
  • Twig Clinics B.V.

    Bilthoven

    Patrick de Zeeuw, Doctor of Philosophy, ‭(0348) 78 81 08‬, p.dezeeuw@twigclinics.com

    Recruiting
  • Molemann Mental Health

    Hilversum

    Anneke Legters, 035-6426000, Anneke.Legters@MoleMann.nl

    Recruiting
  • Twig Clinics B.V.

    Woerden

    Patrick de Zeeuw, Doctor of Philosophy, 0348 788 108, p.dezeeuw@twigclinics.com

    Recruiting

Other trials in Netherlands

About this study

HmT/LmG is a group course for 4-6 parental dyads and consists of 4 group sessions with psycho-education and skills training and 3 individual sessions per family (i.e., 1 session with the adolescent, 1 session with the parents, and 1 session with parents and adolescent together). We want to evaluate effectiveness and treatment process mechanisms applying self-reports, audio observation and interviews.

Read the detailed description

HOLD ME TIGHT/LET ME GO: STUDY PROTOCOL (version 2025-05-01) Participants In- and exclusion criteria will be determined with unstructured clinical interviews by experienced clinicians during the screening.

Inclusion criteria:

  1. Families with one or both parents/primary caretaker (single parent or blended families are allowed) with one adolescent of 12 to 18 years of age;
  2. Adolescent problems are deemed to be exacerbated by a stressful parent-adolescent relationship.

Exclusion criteria:

  1. Participants in command of the Dutch language.
  2. Parents/primary caretakers and adolescents with severe psychopathology (e.g., psychosis, acute suicidality, severe depression) that will interfere with participation in the program.
  3. Parents/primary caretakers already attending systemic therapy or intensive parental guidance during the waiting period and during HmT/LmG. Other individual therapy will be registered during intake, and afterwards by the therapists. During follow-up systemic interventions are allowed but have to be registered.

Design A randomized design comparing the intervention with a control group is not deemed feasible as this requires the simultaneous consent of families (i.e., father, mother and adolescent) to be randomized, which is much harder to achieve than with individuals. Further, the group format of the program (4 to 6 families) requires randomization of 8 to 12 families to be completed within a reasonable time frame otherwise families that were first randomized may drop out. From earlier experiences with randomization of groups of couples is known that this is not feasible because it will compromise inclusion unacceptably. Moreover, it was concluded that studies aiming at relationship enhancement may not need to include waitlist control groups as two meta-analyses found no statistically significant spontaneous improvement from relational problems (Baucom et al., 2003; Roddy et al., 2020). This is in contrast with depression which is known for its high spontaneous remission rates.

All in all, a within-subjects design will be used in which families serve as their own controls with three waves: waiting-period, treatment and follow-up. The waiting period will span on average five weeks (i.e., two to eight weeks), the treatment phase will last about 6 weeks, followed by a follow-up period of about 8 weeks). Change across the three waves will be compared. Little change is anticipated little change during the waiting period (indicating no spontaneous remission), gain during treatment, and little change (substantial maintenance) during follow-up.

Hypotheses:

  1. ∆ waiting period < ∆ intervention period
  2. M post-intervention period ≈ M follow-up period To enable these comparisons all questionnaires must be administered at least four times (pre-waiting, pre-treatment, post-treatment, follow-up)

Procedure: intervention and assessments

The intervention is a course for groups of parents from 4-6 families to help them to enhance their relationship with their adolescent child. The procedure plus timeline for parents and adolescents will be:

  1. Parents intake session (8 to 2 weeks prior to session 1, duration 45-60 min.) is part of the standard procedure of the participating clinical practice. Goal: determining whether parents and adolescent are eligible for the HmT/LmG program. Measurements: (a) parents: paper and pencil (14 min., see measurement scheme parents), and (b) adolescent: paper and pencil when coming along with the parents otherwise via Qualtrics (11 min., see measurement scheme adolescents).
  2. Parents group session 1 (2 to 8 weeks after intake, duration 150 min.). Goal: parents receive psycho-education about: (a) basic adolescent's needs (safe bonding with parents, validation, and autonomy to discover their identity), (b) the importance of parents being open and helpful (the building blocks of secure attachment) to facilitate fulfillment of the adolescent's needs, and (c) recognition of negative parent-adolescent interaction patterns that thwart need fulfillment. Exercises and role play on recognition of negative patterns and their effects are included. Measurement: (a) parents: paper and pencil (14 min.), and (b) adolescent: Qualtrics (11 min.).
  3. Parents group session 2 (1 week after session 1, duration: 150 min.). Goal: parents receive psycho-education about: (a) self-protective behavior modes that underlie the negative interaction pattern, (b) attachment underlying self-protective behavior, (c) how to de-escalate and validate their adolescent. Exercises and role play on validation are included. Measurement: (a) parents: paper \& pencil (5 min.).
  4. Parents group session 3 (2 weeks after session 2, duration: 150 min.). Goal: parents receive psycho-education about: (a) stop escalation and start being open and helpful, (b) apologizing when the negative patterns re-emerges, ad (c) limit-setting to their adolescent. Exercises and role play on apologizing and limit setting are included. Measurements: (a) parents: paper \& pencil (6 min.).
  5. Adolescent individual session (between group sessions 3 and 4, duration: 30-45 min.). Goal: adolescent interviewed by EFT therapist about: (a) negative patterns with the parents, and (b) unfulfilled needs. Measurement: (a) adolescent: live Qualtrics (8 min.). PhD student will take care of this.
  6. Parents individual session (between group sessions 3 and 4, duration: 90 minutes). Goal: parents are prepared by an EFT therapist to a conversation with their adolescent aiming at restoring: (a) staying open and helpful, (b) help their adolescent to fulfil their needs, (c) without relapsing into the negative pattern. Measurement: parents: paper \& pencil (6.5 min.).
  7. Parents-adolescent individual session (between sessions 3 and 4, duration: 90 min.). Goal: restoring the secure bond with parents and adolescents refraining from the negative pattern, and the adolescent is stimulated to be open about his/her unfulfilled needs, while the parents have to stay open \& helpful to the adolescents needs (i.e., repairing the secure bond by the three learned skills apologizing, validating and safe limit setting) Measurements: parents: paper \& pencil (6 min.), and (b) adolescent: paper \& pencil (7 min.), and EFT therapist: (c) audio recording of the session, and (d) scoring the degree of goal attainment for this sessions.
  8. Parents group session 4 (3 weeks after session 3, duration: 150 min.). Goal: parents receive psycho-education about: (a) summary of the core content of the course. Exercises and role play on (aspects) of restoring the secure bond, and reading emotions and facilitation of needs of the adolescent. Measurements: (a) parents: paper \& pencil (12 min.), and (b) adolescent: Qualtrics (11 min.).
  9. Parents-adolescent follow-up interview (8 weeks after session 4, duration 30-60 min.).

Goal: interview with parent(s) and adolescent about working mechanisms of HmT/LmG, testing a (initial) program theory (realist evaluation) to identify causal processes by examining how the program outcomes are caused by which underlying mechanisms within specific contexts.

Measurements: parents: live Qualtrics (12 min.), and (b) adolescent: live Qualtrics (11 min.), and (c) parents and adolescent: record of live qualitative interview via Zoom (30-60 min.).

Being tested
Hold me Tight / Let me Go
Keywords
Hold Me Tight Program, Emotionally Focused Therapy, Parent Child Problems, Parent Child Relationships, Adolescents

What participants receive

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

  • Hold me Tight / Let me GoBehavioural

    Hold Me Tight / Let Me Go (HmT/LmG) is a manualized, group-based behavioral intervention for parents of adolescents aged 12 to 18. Grounded in Emotionally Focused Therapy (EFT) and Hold me Tight for couples. HmT/LmG aims to improve the parent-adolescent relationship by enhancing emotional validation, secure attachment, and effective communication.

    The intervention consists of four group sessions for parents, supplemented by three structured individual or dyadic sessions involving both parents and adolescents. Key components include psycho-education, role plays, emotion-focused conversations, and exercises targeting validation, apologizing, and supportive limit setting. Families complete pre- and post-intervention questionnaires and a follow-up assessment to evaluate changes in relationship quality and psychological well-being.

What is being measured

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

  1. Change in relationship satisfaction (CSI-4)

    Positive change in relationship satisfaction of partners and adolescents (partners will report about their partner relationship, and parents and adolescents report about the parent-adolescent relationship). Satisfaction with the partner relationship of the parents, and the parent-adolescent relationship will be assessed with the 4 item Couple Satisfaction Index (CSI-4; Funk \& Rogge, 2007).

    Funk, J. L., \& Rogge, R. D. (2007). Testing the ruler with item response theory: Increasing precision of measurement for relationship satisfaction with the Couples Satisfaction Index. Journal of Family Psychology, 21(4), 572-583. https://doi.org/10.1037/0893-3200.21.4.572

    Measured: Change from baseline (pre-waiting, week 0) to post-intervention (week 5) and follow-up (week 13)

  2. Change in negative patterns (RDS)

    Negative change in negative patterns of partners and parents (partners will report about their partner relationship and parents and adolescents report about the parent-adolescent relationship). Negative patterns between the parents as partners and between parents and adolescent will be measured by the Relationship Dynamics Scale (RDS; Stanley et al., 2006) a four item self-report questionnaire. An example item is: 'When we argue, one of us withdraws, that is, does not want to talk about it anymore or leaves the scene.'

    Stanley, S. M., Amato, P. R., Johnson, C. A., \& Markman, H. J. (2006). Premarital education, marital quality, and marital stability: Findings from a large, random household survey. Journal of Family Psychology, 20(1), 117-126. https://doi.org/10.1037/0893-3200.20.1.117

    Measured: Change from baseline (pre-waiting, week 0) to post-intervention (week 5) and follow-up (week 13)

Secondary outcomes (4)
  1. Adolescents psychological need fulfillment (BPNS-9)

    Increase in psychological need fulfillment of adolescents (adolescents will report about themselves). Need fulfillment in the context of the parent-adolescent relationships will be measured with the 9 item Basic Psychological Need Satisfaction in Relationships scale (BPNS-R). The adolescent version is based on the partner version (La Guardia, Ryan, Couchman, \& Deci, 2000) and inspired in its wording by the Flemish version (Van der Kaap-Deeder et., 2020).

    La Guardia, J. G., Ryan, R. M., Couchman, C. E., \& Deci, E. L. (2000). Within-person variation in security of attachment: A self-determination theory perspective on attachment, need fulfillment, and well-being. Journal of Personality and Social Psychology, 79, 367-384. http://doi.org/dhghf4

    Van der Kaap-Deeder, J., Soenens, B., Ryan, R. M., \& Vansteenkiste, M. (2020). Manual of the Basic Psychological Need Satisfaction and Frustration Scale (BPNSFS). Ghent University, Belgium.

    Measured: Change from baseline (pre-waiting, week 0) to post-intervention (week 5) and follow-up (week 13)

  2. Adolescents support seeking to parent (IERQ-3)

    Increase in support seeking behavior of partners and adolescents (parents will report about their partner relationship and adolescents about the parent-adolescent relationship). Support seeking will be measured with a slightly adapted version of the Soothing subscale of the Interpersonal Emotion Regulation Questionnaire (IERQ; Hofman et al., 2016). We shortened the original version from five to three items and adapted the wording from referring to 'others' into the partner or one of the parents.

    Hofmann, S. G., Carpenter, J. K., \& Curtiss, J. (2016). Interpersonal Emotion Regulation Questionnaire (IERQ): Scale development and psychometric characteristics. Cognitive Therapy and Research, 40(3), 341-356. https://doi.org/10.1007/s10608-016-9756-2

    Measured: Change from baseline (pre-waiting, week 0) to post-intervention (week 5) and follow-up (week 13)

  3. Adolescents quality of life (KIDSCREEN-10)

    Increase in quality of life of adolescents (parents and adolescent will report about adolescent). Quality of life in terms of physical, mental, and social well-being will be determined by both the official parental and adolescent versions of the KIDSCREEN-10 (Ravens-Sieberer, 2006).

    Ravens-Sieberer, U. The Kidscreen Questionnaires: Quality of Life Questionnaires for Children and Adolescents; handbook; Pabst Science Publ.: Lengerich, Germany, 2006.

    Measured: Change from baseline (pre-waiting, week 0) to post-intervention (week 5) and follow-up (week 13)

  4. Perceived ARE from parent to adolescent (BARE-6)

    Increase in the accessibility and responsiveness of partners and parents (partners will report about their partner and adolescents and parents about the parent). Accessibility and responsiveness to the partner's and adolescent's needs will be assessed with the 6 item Brief Accessibility, Responsiveness and Engagement scale (BARE: Sandberg et al., 2012).

    Sandberg, J. G., Busby, D. M., Johnson, S. M., \& Yoshida, K. (2012). The Brief Accessibility, Responsiveness, and Engagement (BARE) Scale: A tool for measuring attachment behavior in couple relationships. Family Process, 51(4), 512-526. https://doi.org/10.1111/j.1545-5300.2012.01422.x

    Measured: Change from baseline (pre-waiting, week 0) to post-intervention (week 5) and follow-up (week 13)

Timeline

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

  1. First posted11 May 2025
  2. Study start11 Jun 2025
  3. Primary completion1 Feb 2028 (estimated)
  4. Study completion1 Sep 2028 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
150 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06966323
Sponsor's protocol ID
FMG-12034
Status last verified
Dec 2025
First submitted
2 May 2025
Last updated
24 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Currently decided that individual participant data (IPD) will not be shared due to the sensitive nature of the data, which involves minors and families in a clinical setting. Ensuring participant confidentiality is a priority, and current infrastructure does not support secure sharing of these data. Future data sharing may be considered if appropriate anonymization and data use agreements can be established.

Questions about this trial

What is this clinical trial studying?

An observational study of Parent Training and Parent Child Relationship, run by University of Amsterdam at 5 sites in Netherlands.

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

Who may be eligible to take part?

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: looking for participants now, as of the sponsor's last update on 24 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in Netherlands. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Sophie Jonker, Master of Science (31652365964, s.jonker@uva.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in relationship satisfaction (CSI-4) (time frame: Change from baseline (pre-waiting, week 0) to post-intervention (week 5) and follow-up (week 13)). The study lists 2 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 24 Dec 2025.

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