NCT05477420

Brief Summary

The goals of this study is to examine whether treatment preferences shift after receiving a clients' decision aids about psychotherapy in digital and in in-person format.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
148

participants targeted

Target at P50-P75 for not_applicable depression

Timeline
Completed

Started Mar 2022

Typical duration for not_applicable depression

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 20, 2022

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

July 6, 2022

Completed
22 days until next milestone

First Posted

Study publicly available on registry

July 28, 2022

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 10, 2024

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 20, 2024

Completed
Last Updated

December 27, 2024

Status Verified

December 1, 2024

Enrollment Period

2.3 years

First QC Date

July 6, 2022

Last Update Submit

December 21, 2024

Conditions

Keywords

DepressionOnline psychotherapiespsychotherapiesDecision aid

Outcome Measures

Primary Outcomes (1)

  • Decisional conflict

    The decisional conflict scale (DCS) SURE-test

    Immediately before and right after (within 10 mins) the completion of the intervention.

Secondary Outcomes (4)

  • Stage of decision making

    Immediately before and right after (within 10 mins) the completion of the intervention.

  • Satisfaction with Decision (SWD) Scale

    Immediately before and right after (within 10 mins) the completion of the intervention.

  • Perceived benefits and risks

    Immediately before and right after (within 10 mins) the completion of the intervention.

  • Service Preference Identity

    Immediately before and right after (within 10 mins) the completion of the intervention.

Other Outcomes (1)

  • Depressive symtoms

    Before intervention

Study Arms (2)

Experimental group

EXPERIMENTAL

Participants in the experimental group will be expected use the decision aid developed in this study. They will be assessed at two different time points: (1) before intervention (T0) and (2) post-intervention (T1).

Other: Decision Aid

Attention control group

NO INTERVENTION

The control group participants will be asked to search information related to "Depression" and "therapies for Depression" online. They will be assessed at two different time points: (1) at baseline (T0) and (2) after searching for information (T1).

Interventions

Participants in the experimental group would be asked to use the decision aid developed by the study. The decision aid tool will ask participants their preferences on traditional face-to-face and online psychotherapies and how they rank different treatment attributes.

Experimental group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being 18 years of age or older;
  • With at least mild to moderate depressive symptoms (defined as having a cut-off score of 10 or above based on the PHQ-9, Patient Health Questionnaire-9)
  • Being Chinese speaking

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Psychology

Hong Kong, Hong Kong

Location

Related Publications (56)

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MeSH Terms

Conditions

Depression

Interventions

Decision Support Techniques

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Investigative Techniques

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

July 6, 2022

First Posted

July 28, 2022

Study Start

March 20, 2022

Primary Completion

July 10, 2024

Study Completion

December 20, 2024

Last Updated

December 27, 2024

Record last verified: 2024-12

Locations