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Completed

NCT Number: NCT06456775

Tele-SSM: A Telephone Technology Innovation in the Intervention on Supported Self-management for Depression in Vietnam

Tele-SSM is a pre-post mixed-method study to investigate the feasibility, acceptability and the preliminary efficacy of the support self-management skills intervention for depression delivered from distance.

The specific objectives of this research include:

* Transform the SSM intervention for depression from face-to-face delivery to delivery from distance. * Develop an software for intervention management * Examine knowledge, attitudes and practices of people with depression toward depression * Examine the feasibility, acceptability and preliminary efficacy of the intervention * Investigate the cost analysis of Tele-SSM intervention

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Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute for Social Development Studies

Hanoi, 10000, Vietnam

About this study

Introduction

In the context of limited interventions for depression in Vietnam and the strong potential for tele-health to improve accessibility to mental health care in low-middle income countries, the principal investigators conducted a pre-post mixed-method study of a supported self-management for depression delivered from distance (Tele-SSM) to evaluate the preliminary efficacy, feasibility and acceptability of this approach on depression and other mental health outcomes for adults with depression symptoms in Vietnam and to explore knowledge, attitudes and practices of people with depression towards depression.

Method

This is pre-post mixed method study. The princial investigators use both quantitative and quanlitative methodology to evaluate the preliminary efficacy, feasibility and acceptability of Tele-SSM intervention on depression and other mental health outcomes for adults with depression symptoms in Vietnam and to explore knowledge, attitudes and practices of people with depression towards depression.

Recruitment

Participants ages 18-64 years ared recruited online through social media from May 2022 and May 2023. Interested participants completed the PHQ-9 on Kobotoolbox. Potential participants who satisfy the eligibility criteria of the study provided contact information. A research assistant with a psychology background conducted a video call with each potential participant to confirm their eligibility, provide information about the study and the intervention. Informed consent was obtained from all individual participants included in the study.

All procedures performed in studies involving human participants are in accordance with the ethical standards of the institutional ethical committee and was approved by the Institutional Review Board at ISDS (IRB00011703) on 05th May 2021 in Hanoi.

Sample size considerations

Findings from meta-analytic studies examining the effect of CBT interventions indicate the effect size for CBT on depressive symptoms to be 0.53 (Cuijpers et al., 2013) and on health-related quality of life to be 0.63 (Hofmann et al., 2017). Sample size calculations indicated that a sample size of 52 participants was sufficient to detect a conservative anticipated effect size of 0.40, with a statistical power of 80% and a two-sided alpha level of 0.05. The target sample size was increased to 72, assuming an anticipated attrition rate of 20%. In reality, the principal investigators recruited 75 patients, with 58 patients completing the intervention.

Data management

  • Participants completed pre- and post-questionnaires online using Kobotoolbox. The in-depth interviews are audio-recorded. Audio recordings are transcribed. Participant records are managed by a secured website.

Data Analysis Plan

  • Qualitative analysis methods: The IDIs are audio-recorded, transcribed and analyzed thematically to identify significant themes, patterns, and potential correlational relationships. The analysis is conducted with Excel software.
  • Quantitative analysis method: The principal investigators calculate descriptive statistics for all variables (means, ranges, standard deviations, percent data missing, and frequencies for categorical variables). For continuous variables, the principal investigators conduct statiscial tests to test for differences before and after intervention. For the acceptability, frequencies for questions on satisfaction were calculated from endline data.
  • Cost analysis method: The principal investigators analyze all costs incurred from activities of Tele-SSM intervention for all participants in the study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged from 18-64 years
  • Have a score of PHQ-9 (26) greater than 5.

Exclusion criteria

  • Any participants with severe mental health problems i.e. schizophrenia, bipolar disorder, recent suicide attempts and/or with suicide plans were excluded (current suicide ideation, but without recent suicide attempts and/or with suicide plans were not excluded).

Treatment and study plan

Tele-SSM

Behavioral

Tele-SSM an individual-level psychosocial intervention based on cognitive behavior therapy principles and non-violent communication. The intervention consists of the following 10 sessions delivered through 10 weekly coaching calls delivered by Zoom (audio only).

Primary outcomes

  1. Depression

    Time frame: Pre intervention and up to 12 weeks

    Measured by PHQ-9 questionnaire

  2. Acceptability

    Time frame: Up to 12 weeks after pre-intervention survey

    Measured by questionnaire and in-depth interviews

  3. Feasiblity

    Time frame: Up to 12 weeks after pre-intervention survey

    Measured by questionnaire and in-depth interviews

  4. Cost

    Time frame: Through study completion, an average 6 months

    Measured by financial reports

Secondary outcomes

  1. Anxiety

    Time frame: Pre intervention and up to 12 weeks

    Measure by DASS-21 questionnaire

  2. Stress

    Time frame: Pre intervention and up to 12 weeks

    Measured by DASS-21 questionnaire

  3. Self-esteem

    Time frame: Pre intervention and up to 12 weeks

    Measured by Rosenberg self - Esteem scale

  4. Social support

    Time frame: Pre intervention and up to 12 weeks

    Measured by Multidimensional Scale of Perceived Social Support (MSPSS)

  5. Health related quality of life

    Time frame: Pre intervention and up to 12 weeks

    Measured by SF-12 and EQ-5D-5L questionnaire

  6. Knowledge, attitude and practices of people with depression

    Time frame: Pre-intervention

    Measured by in-depth interviews

Sponsors and collaborators

Lead sponsor

Institute for Social Development Studies, Vietnam

Other

Collaborators

  • National Foundation for Science & Technology Development, Vietnam

Registry information

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Jun 13, 2024
Registry last updated
Jun 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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