Effectiveness of a Psychological Intervention to Reduce Social Isolation and Promote Social Connectedness in Young Adults
The purpose of this randomized controlled trial is to evaluate the effectiveness of a psychological intervention aimed at reducing social isolation and promoting social connectedness among young adults. Specifically, the study investigates the impact of an 8-week, digitally assisted face-to-face group social skills training program on individuals aged 19 to 34 who experience difficulties in interpersonal relationships and social isolation. Participants will be randomly assigned to either the active intervention group or a waitlist control group. The study aims to determine whether this structured psychosocial intervention improves interpersonal competence and social performance, reduces social isolation, and improves other psychosocial variables. Outcomes will be evaluated at three time points-pre-intervention, post-intervention, and a 1-month follow-up-utilizing a combination of self-report questionnaires and performance-based role-play assessments.
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Jaehee Jung
- Telefonnummer: 821073177521
- E-Mail: emqhfkwogml13@gmail.com
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Adults aged 19 to 34 years
- South Korean nationality
- Interpersonal Competence Questionnaire, 15-item short form (ICQ-15): mean score of 2.87 or lower
- Meets either (a) or (b) below:
- (a) Lubben Social Network Scale-6 (LSNS-6) total score of less than 12, AND short-form UCLA Loneliness Scale-8 total score of 17 or higher
- (b) Korea University Social Isolation Scale (KUSIS) total score of 9 or higher
- Confirmation on a non-face-to-face screening interview that the participant's primary difficulty involves interpersonal problems stemming from a lack of social knowledge and skills
Exclusion Criteria:
- Psychiatric or neurological hospitalization within the past 6 months
- Current or past diagnosis of a severe neurological disorder
- Cognitive impairment severe enough to hinder the basic communication required for program participation
- Suicide attempt within the past 6 months
- Severe suicide risk identified during the assessment
- History of psychotic symptoms or manic episodes
- Severe psychiatric condition or major medical abnormality that would complicate participation
- Unable or unwilling to follow the research team's instructions during the application process
- Currently participating in individual or group psychotherapy that provides training in other social skills
- Participation within the past 5 years in a study on social isolation conducted by an investigator of the present research team, which raises concern for a confounding effect on the study results
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
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Kein Eingriff: Wartelistenkontrolle
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Experimental: Digital-Assisted Group Social Skills Training
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Participants assigned to the active intervention arm receive an 8-week, face-to-face group social skills training program, which involves weekly 120-minute sessions supplemented by a web-based digital platform designed to promote between-session practice and skill generalization. |
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Korean Version of the Interpersonal Competence Questionnaire (K-ICQ)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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The Korean Version of the Interpersonal Competence Questionnaire (K-ICQ) is a 31-item self-report measure of interpersonal competence. Each item is rated on a 5-point Likert scale from 1 (poor) to 5 (extremely good). The total score sums all items and ranges from 31 to 155. Higher scores indicate greater interpersonal competence, which is a better outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Social Skills Knowledge Test
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Social Skills Knowledge Test is an investigator-developed knowledge test created to objectively measure acquisition of the social skills content taught in the intervention. It consists of 21 items (multiple-choice and true/false) covering seven domains that correspond to the session curriculum: relationship formation skills, conversation skills I, conversation skills II, assertion skills, conflict management skills, dating skills, and workplace skills, with 3 items per domain. Each item has an unambiguously correct answer and is scored 1 (correct) or 0 (incorrect). The total score is the sum of correct responses and ranges from 0 to 21. Higher scores indicate greater knowledge of social skills, which is a better outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Korea University Social Isolation Scale (KUSIS)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Korea University Social Isolation Scale (KUSIS) is a 9-item self-report measure of social isolation risk. Respondents rate their state over the past month, excluding people they currently live with. Each item is rated on a 4-point scale from 0 (never) to 3 (very much). The total score sums all items and ranges from 0 to 27, with a cut-off of 9 or higher indicating risk of social isolation. Higher scores indicate greater social isolation, which is a worse outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Lubben Social Network Scale-6 (LSNS-6)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Lubben Social Network Scale-6 (LSNS-6) is a 6-item self-report measure of social network size and engagement; three items concern family and relatives, and three concern friends and other acquaintances. Each item is rated on a 6-point scale from 0 (none) to 5 (nine or more people). The total score sums all items and ranges from 0 to 30. Higher scores indicate a larger and more engaged social network, which is a better outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Short-form UCLA Loneliness Scale-8
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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The short-form UCLA Loneliness Scale-8 (ULS-8) is an 8-item self-report measure of loneliness abbreviated from the 20-item UCLA Loneliness Scale. Each item is rated on a 4-point scale from 1 (never) to 4 (always); two positively worded items are reverse-scored. The total score is the sum of all items and ranges from 8 to 32. Higher scores indicate greater loneliness, which is a worse outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
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Patient Health Questionnaire-9 (PHQ-9)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Patient Health Questionnaire-9 (PHQ-9) is a 9-item self-report measure of depressive symptoms over the preceding two weeks, based on the DSM-IV diagnostic criteria for major depressive disorder. Each item is rated on a 4-point scale from 0 (not at all) to 3 (nearly every day). The total score is the sum of all items and ranges from 0 to 27. Higher scores indicate more severe depressive symptoms, which is a worse outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Generalized Anxiety Disorder-7 (GAD-7)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Generalized Anxiety Disorder-7 (GAD-7) is a 7-item self-report measure of the core symptoms of generalized anxiety disorder over the preceding two weeks. Each item is rated on a 4-point scale from 0 (not at all) to 3 (nearly every day). The total score is the sum of all items and ranges from 0 to 21. Higher scores indicate more severe anxiety symptoms, which is a worse outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Korean version of the Social Interaction Anxiety Scale-Social Phobia Scale Short Form (K-SIAS-SPS-SF)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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The Korean version of the Social Interaction Anxiety Scale-Social Phobia Scale Short Form (K-SIAS-SPS-SF) is a single 14-item self-report measure of social anxiety. Its items were derived by exploratory factor analysis of the pooled 40-item set of the Social Interaction Anxiety Scale and the Social Phobia Scale, and the resulting instrument is administered and scored as one scale comprising three correlated factors: social interaction anxiety (5 items), fear of overt evaluation (6 items), and fear of attracting attention (3 items). Each item is rated on a 5-point scale from 0 (not at all characteristic of me) to 4 (extremely characteristic of me). A single total score is obtained by summing all 14 items and ranges from 0 to 56, with a total score of 22 or higher indicating probable social anxiety disorder. Higher scores indicate greater social anxiety, which is a worse outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Mental Health Continuum-Short Form (MHC-SF)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Mental Health Continuum-Short Form (MHC-SF) is a 14-item self-report measure of positive mental health over the past month, comprising three subscales: emotional well-being (3 items), social well-being (5 items), and psychological well-being (6 items). Each item is rated on a 6-point frequency scale from 0 (never) to 5 (every day). The total score sums all items and ranges from 0 to 70. Higher scores indicate greater well-being, which is a better outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Multidimensional Scale of Perceived Social Support (MSPSS)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Multidimensional Scale of Perceived Social Support (MSPSS) is a 12-item self-report measure of perceived social support from three sources: significant other, family, and friends, with 4 items per source. Each item is rated on a 7-point Likert scale from 1 (very strongly disagree) to 7 (very strongly agree). The total score sums all items and ranges from 12 to 84. Higher scores indicate greater perceived social support, which is a better outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
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Broad Autism Phenotype Questionnaire Short Form (BAPQ-SF)
Zeitfenster: Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
The Broad Autism Phenotype Questionnaire Short Form (BAPQ-SF) is a 14-item self-report measure that assesses core features of the autism spectrum as a continuous dimension in the general population. Each item is rated on a 6-point frequency scale from 1 (very rarely) to 6 (very often), and positively worded items are reverse-scored so that higher values reflect more pronounced traits. The total score sums all items and ranges from 14 to 84. Higher scores indicate more pronounced broad autism phenotype traits, which is a worse outcome. |
Baseline, immediately post-intervention (at 8 weeks), and 1-month follow-up (at 12 weeks)
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- KUIRB-2026-0388
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