Skip to content

A randomised controlled trial investigating the effectiveness of cognitive behavior group therapy compared to a wait list control in the treatment of university students with social phobia

A randomised controlled trial investigating the effectiveness of cognitive behavior group therapy compared to a wait list control in the treatment of university students with social phobia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2015/013
Enrollment
Unknown
Registered
2015-07-13
Start date
2015-08-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Social Phobia

Interventions

Participants would be seen at a community setting (non-hospital based) at the Faculty of Medicine, University of Kelaniya, and the University of Moratuwa Participants meeting the inclusion/exclusion

Sponsors

National Research Council, Sri Lanka
Lead Sponsor
University of Kelaniya, Sri Lanka
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Consenting males and females above 18 years of age 2. Current registration as an undergraduate student of University of Kelaniya or the University of Moratuwa 3. Score of 6 or more in the Mini-Social Phobia Inventory(Mini-SPIN), then confirmed by the Liebowitz Social Anxiety Scale- Self Rated version (LSAS -SR, a score of 55 or more) and the social phobia criteria of the Mini-International Neuropsychiatric Interview (M.I.N.I.) 4. Score of less than 70 on the Zung Depression rating scale and score less than 3 suicidal ideas (on item 19) of the Zung depression rating scale

Exclusion criteria

Exclusion criteria: 1. Currently undegoing CBT with psychologist or another healthcare professional 2. Currently on a medication for social phobia (selective Serotonine Reuptake Inhibitor/Tricyclic antidepressant/ Benzodiazepines) 3. At risk of self-harm or suicide 4. Current or past diagnosis of psychosis, schizophrenia or bipolar disorder 5. Primary diagnosis of major depressive disorder, panic disorder, obsessive compulsive disorder, post-traumatic stress disorder or substance dependence 6. Planning to become pregnant or if pregnant or breastfeeding

Design outcomes

Primary

MeasureTime frame
Level of anxiety symptoms as indexed by scale scores on the LSAS-SR, CGI before and after group Cognitive Behavioural Therapy [At baseline, one week, six weeks, 12 weeks from the commencement of the study.] Salivary cortisol levels before and after group Cognitive Behavioural Therapy [At baseline, one week, six weeks, 12 weeks from the commencement of the study.]

Secondary

MeasureTime frame
None [None]

Countries

Sri Lanka

Contacts

Public ContactDr.Aruni Hapangama

Senior Lecturer

Email: ahapangama@yahoo.co.ukTel: 0777917311

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Aug 9, 2026