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RecruitingNCT06521099Updated Sep 10, 2026

A Novel Conditioning Approach to Counter Loneliness in Adults

An interventional study of Evaluative Conditioning with positive stimuli and Conditioning with neutral stimuli in Loneliness, sponsored by Education University of Hong Kong. Recruiting at 1 site in Hong Kong. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-10.

Sponsored by Education University of Hong Kong · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2025; still recruiting 1 year 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
136
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study aims to test the efficacy of a 6-session conditioning paradigm by investigating the conditioning-induced change in the socio-affective processing, loneliness, depressive symptoms, and neural correlates of lonely adults.

Read the detailed description

Potential participants will first be invited to complete a loneliness questionnaire online. Lonely adults will then be invited to undergo further screening. At baseline prior to the intervention training sessions, participants will first complete tests and questionnaires on loneliness, mood and depressive symptoms in addition to other socio-affective measures, and they will also be invited to receive resting-state functional MRI scanning in a 3T MRI scanner. Participants will then be allocated to one of the two intervention arms (the evaluative conditioning, and the control) in a randomized fashion with approximately half in each group. They will then complete the pre-conditioning phase of the allocated intervention arm, and their ratings on the stimuli presented during this phase will be assessed. In the conditioning phase, they will be invited to attend 6 sessions. After completing the conditioning phase, participants will be invited to complete the post- conditioning phase, providing ratings on the stimuli like the pre-conditioning phase. Immediately after, and also 3 months after, participants will be invited to complete again tests and questionnaires on loneliness, mood and depressive symptoms in addition to other socio-affective measures, and they will also be invited to receive resting-state functional MRI scanning in a 3T MRI scanner.

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Conditions studied

  • Loneliness
03

In context

Lead sponsor

Education University of Hong Kong is the lead sponsor of 35 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • No histories of learning impairment, major psychiatric disorders or neurological disorders other than depression
  • Normal intelligence
  • At least primary school education

Exclusion criteria

Exclusion Criteria:

  • On medication or treatments within 2 weeks prior to the beginning of the study that would affect the individual's brain, cognitive and affective functions
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
136 participants (estimated)

Study arms

  • Experimental
    Evaluative conditioning group with positive stimuli

    Participants will be exposed to social stimuli paired with positive stimuli across multiple sessions.

    Behavioral: Evaluative Conditioning with positive stimuli

  • Active comparator
    Control group with neutral stimuli

    Participants will be exposed to social stimuli paired with neutral stimuli across multiple sessions.

    Behavioral: Conditioning with neutral stimuli

Interventions

  • BehavioralEvaluative Conditioning with positive stimuli

    In the pre-conditioning phase, participants will be exposed to pictures that vary in their emotional (negative, positive) and social (non-social, social) content. For each picture, they are required to indicate their immediate perceived valence (between negative to positive), degree of social motivation (between none to high) on Likert-scales. In the conditioning phase, emotional social pictures will be selected and paired with non-social positive stimuli for trials in random order, for 6 sessions across 3 weeks. In the post-conditioning phase, participants will be asked to evaluate the valence of the stimuli again similar to that in pre-conditioning phase.

  • BehavioralConditioning with neutral stimuli

    In the pre-conditioning phase, participants will be exposed to pictures that vary in their emotional (negative, positive) and social (non-social, social) content. For each picture, they are required to indicate their immediate perceived valence (between negative to positive), degree of social motivation (between none to high) on Likert-scales. In the conditioning phase, emotional social pictures will be selected and paired with with neutral non-social stimuli for trials in random order, for 6 sessions across 3 weeks. In the post-conditioning phase, participants will be asked to evaluate the valence of the stimuli again similar to that in pre-conditioning phase.

06

What researchers measure

Primary outcomes

  1. Self-reported loneliness

    Loneliness is assessed based on the UCLA loneliness scale (Version 3), a 20-item 4-point Likert scale (score range 20 - 80) in which higher scores indicate greater degrees of loneliness.

    Time frame: Baseline, immediately after, and 3 months after the intervention

  2. Implicit loneliness

    Implicit loneliness will be measured by Implicit Association Test about the relative strength of association between our participants' target concept 'Self' and attribute 'Lonely'.

    Time frame: Baseline, immediately after, and 3 months after the intervention

Secondary outcomes

  1. Valence of social stimuli

    For each stimuli, they are required to indicate their immediate perceived valence (between negative to positive) of the scenes on a 7-point Likert scale (1 = strongly positive, 7 = strongly negative).

    Time frame: Baseline, immediately after, and 3 months after the intervention

  2. Social motivation towards social stimuli

    For each stimuli, they are required to indicate their immediate perceived degree of social motivation (between none to high) of the scenes on a 7-point Likert scales (1 = no, 7 = very high).

    Time frame: Baseline, immediately after, and 3 months after the intervention

  3. Loneliness-related activation patterns and connectivity in neural networks

    Neural connectivity in Default Mode Network, Ventral Attention Network, Frontoparietal Network are assessed by fMRI

    Time frame: Baseline, immediately after, and 3 months after the intervention

  4. Depressive symptoms

    Depressive symptoms are assessed based on the Hospital Anxiety and Depression Scale, a 14-item scale assessing severity of depressive and anxiety symptom (score range 0 - 21 for both subscale), with higher scores indicating higher severity

    Time frame: Baseline, immediately after, and 3 months after the intervention

  5. Daily loneliness

    Daily loneliness is assessed based on a 5-minute self-report on a Likert scale

    Time frame: Through study completion, on average of 4 months

07

Study locations

1 of 1 sites recruiting
  • The University of Hong Kong
    Hong Kong, Hong Kong
    Recruiting
08

References and documents

Publications

  • Wong NML, Lee TMC. Evaluating the effects of a conditioning training paradigm on loneliness, socio-affective processing, and brain connectivity: a study protocol of a two-arm randomised controlled trial. BMC Psychol. 2025 Aug 27;13(1):975. doi: 10.1186/s40359-025-03342-3. PubMed 40866945 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06521099
Lead sponsor
Education University of Hong Kong
Collaborators
The University of Hong Kong
Responsible party
WONG Man Lok Nichol (Assistant Professor, Education University of Hong Kong) — Principal investigator
First posted
Jul 25, 2024
Start date
Aug 19, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Sep 10, 2026

Study contacts

Nichol ML Wong, PhD
Contact
nmlwong@eduhk.hk
852-29487431
Nichol ML Wong, PhD
principal investigator · Education University of Hong Kong

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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