CClinicalTrials.gg
Not yet recruitingNCT07288671Updated Dec 23, 2025

Nostalgia Intervention on Alleviating Loneliness Amongst Older Adults

An interventional study of Nostalgia intervention in Loneliness, sponsored by Chinese University of Hong Kong. Not yet recruiting. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2025-12-23.

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

Phase
Not applicable
Study type
Interventional
Enrollment
294
Allocation
Randomized
Ages
60 Years and older
Sex
All
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Study summary

The proposed study will utilise a two-arm, cluster-randomised, waitlist-controlled trial to (1) examine the effects of the nostalgia intervention on loneliness, negative emotions, social connectedness, meaning in life and nostalgia amongst community-dwelling older adults in Hong Kong; (2) investigate whether the effect of the nostalgia intervention on loneliness is mediated by improvements in negative emotions, social connectedness and meaning in life; and (3) explore the experiences and perceptions of older adults participating in the nostalgia interventions, focusing on their views regarding the impact of the intervention on their loneliness.

Read the detailed description

A convenience sample of 294 older adults from six participating community centres, with 49 participants from each centre. Eligible older adults will be randomly assigned to either a waitlist control group (n = 147) or an intervention group (n = 147). Both groups will receive standard community support services, whilst the intervention group will also participate in five weekly face-to-face nostalgia sessions (approximately 90 min each) in a group format. Additionally, a purposive subsample of 30 participants from the intervention group will be invited for focus group interviews.

The primary outcome (loneliness) and secondary outcomes will be assessed at baseline (T0), immediately post-intervention (T1), 3 months post-intervention (T2) and 6 months post-intervention (T3) using validated questionnaires. The investigators will analyse the quantitative data using a generalised estimating equation model with intention-to-treat and path analyses. The qualitative data will be analysed using reflexive thematic analysis. The findings of this proposed study will inform healthcare professionals and policymakers, offering practical strategies to combat loneliness in this vulnerable group.

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Conditions studied

  • Loneliness

Keywords

  • loneliness
  • older adults
  • nostalgia intervention
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In context

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.

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

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Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • older adults aged 60 years or above
  • residing in the community
  • capable of speaking and understanding Chinese
  • experiencing loneliness (scoring ≥3 on a three-item loneliness screening scale)

Exclusion criteria

Exclusion Criteria:

  • currently undergoing psychological intervention
  • having a clinical diagnosis of mental illness
  • being cognitively impaired (Abbreviated Mental Test score \<6)
  • having visual/language/communication difficulties
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
294 participants (estimated)

Study arms

  • Experimental
    Experimental: Nostalgia intervention

    In addition to usual community support services, participants in the intervention group will receive the face-to-face nostalgia intervention weekly for 5 weeks (each session lasting approximately 90 minutes), with each group consisting of 5-8 older adults.

    Behavioral: Nostalgia intervention

  • No intervention
    Wait-list control

    Participants in the wait-list control group will receive usual community support services provided by the community centres they belong to.

Interventions

  • BehavioralNostalgia intervention

    Participants in the intervention group will receive the face-to-face nostalgia intervention weekly for 5 weeks (each session lasting approximately 90 minutes), with each group consisting of 5-8 older adults. The intervention consists of 5 sessions: Session 1 (understanding nostalgia and its benefits), Session 2-4 (music/ photos/ meaningful objects and nostalgia), Session 5 (reaffirming the benefits of nostalgia).

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What researchers measure

Primary outcomes

  1. Emotional and social loneliness

    The Chinese version of the De Jong Gierveld Loneliness Scale. This six-item scale scores range from 0 to 6, with higher score indicates higher level of loneliness. This scale demonstrates good internal consistency (Cronbach's α = 0.76) and inter-rater reliability (ICC = 0.98-1.00), as well as a strong correlation with direct assessments of loneliness.

    Time frame: Asessed at baseline (T0), immediate after (T1), 3 months (T2), and 6 months (T3) post-intervention

  2. Existential Loneliness

    Existential Loneliness Questionnaire, which comprises 22 items focused on loneliness in social ties, loneliness in close relationships and the search for meaning in life. The scores range from 22 to 132, higher scores indicate higher level of existential loneliness. The questionnaire also demonstrates good internal consistency (Cronbach's α = 0.90).

    Time frame: Asessed at baseline (T0), immediate after (T1), 3 months (T2), and 6 months (T3) post-intervention

Secondary outcomes

  1. Negative emotions

    The Chinese version of the Depression Anxiety Stress Scale consists of 21 items that assess symptoms of depression (7 items), anxiety (7 items), and stress (7 items). Each subscale scores range from 0 to 21, with higher scores indicating greater levels of negative emotions. The Chinese version demonstrates good internal consistency (Cronbach's α = 0.92 to 0.94).

    Time frame: Asessed at baseline (T0), immediate after (T1), 3 months (T2), and 6 months (T3) post-intervention.

  2. Social connectedness

    The revised Social Connectedness Scale to measure the perceived connection of participants to others in their social environment. This scale comprises 20 items measuring four aspects: belongingness, closeness, support and satisfaction. The scores range from 20 to 120, higher scores indicate greater feelings of social connectedness. This scale demonstrates good internal consistency (Cronbach's α = 0.92) and validity.

    Time frame: Asessed at baseline (T0), immediate after (T1), 3 months (T2), and 6 months (T3) post-intervention

  3. Meaning in life

    Meaning in Life Questionnaire, which comprises 10 items measuring presence for and search for meaning in life, to measure meaning in life. The score ranges from 10 to 70, higher scores indicates stronger sense of meaning in life. The Chinese version demonstrates good internal consistency (Cronbach's α = 0.85).

    Time frame: Asessed at baseline (T0), immediate after (T1), 3 months (T2), and 6 months (T3) post-intervention.

  4. Nostalgia

    The Southampton Nostalgia Scale to measure participants' nostalgia. This scale comprises five items that measure the importance participants attribute to nostalgia and two items related to frequency of nostalgia. The scores range from 7 to 49, higher scores indicate a greater dispositional tendency toward nostalgia. This scale demonstrates good internal consistency (Cronbach's α = 0.93).

    Time frame: Asessed at baseline (T0), immediate after (T1), 3 months (T2), and 6 months (T3) post-intervention

  5. Experiences and perceptions of older adults in intervention group

    Focus group interviews will be conducted to explore the experiences and perceptions of older adults in intervention group regarding their participation in nostalgia interventions and the impact of the intervention on their loneliness using an interview guide.

    Time frame: Assessed within 1 day (T1) after the intervention

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 23, 2025, 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
NCT07288671
Lead sponsor
Chinese University of Hong Kong
Responsible party
Cho Lee Wong (Associate Professor, Chinese University of Hong Kong) — Principal investigator
First posted
Dec 17, 2025
Start date
Sep 1, 2026 (estimated)
Primary completion
Jun 30, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Dec 23, 2025

Study contacts

Cho Lee Wong, PhD
Contact
jojowong@cuhk.edu.hk
+852 39438166
Cho Lee Wong, PhD
principal investigator · The Nethersole School of Nursing, CUHK

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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