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Can a Self-guided Mobile Phone Application Program Improve Wellbeing in University Students

N

National University of Singapore

Status

Not yet enrolling

Conditions

Depression, Anxiety
Perfectionism
Self-Compassion
Shame
Stress

Treatments

Behavioral: Cognitive Behavioural Therapy
Behavioral: Active Control
Behavioral: Self-Compassion

Study type

Interventional

Funder types

Other

Identifiers

NCT05475535
NUS-IRB-2022-307

Details and patient eligibility

About

This study seeks to evaluate and compare the effectiveness of a mobile phone application-based intervention in improving wellbeing in young adults. 400 University students are randomized into 1 of 4 intervention types. Pre, mid and post-intervention outcome measures are compared to determine effectiveness of the various intervention types.

Enrollment

400 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Access to a mobile phone with the following requirements: iPhone 8 and above, or Android 5.2+ (display greater than 5 inches)
  • Have scores of greater than or equal to 29 on the 'Concerns over Mistakes' subscale on the FMPS

Exclusion criteria

  • Participants who do not meet the inclusion criteria
  • Currently pregnant
  • Undergoing psychological treatment or counselling
  • Have any change in psychotropic medication within twelve weeks before starting intervention

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

400 participants in 4 patient groups

Active Control
Active Comparator group
Treatment:
Behavioral: Active Control
Cognitive Behavioural Therapy (CBT)
Experimental group
Treatment:
Behavioral: Cognitive Behavioural Therapy
Self-Compassion (SC)
Experimental group
Treatment:
Behavioral: Self-Compassion
Cognitive Behavioural Therapy and Self-Compassion (CBT+SC)
Experimental group
Treatment:
Behavioral: Cognitive Behavioural Therapy
Behavioral: Self-Compassion

Trial contacts and locations

0

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Central trial contact

Mark Ngoh; Marie Tan

Data sourced from clinicaltrials.gov

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