NCT03216655

Brief Summary

Nowadays, doctors put mental health at a prior place and pay more attention to the psychological problems of ill kids' parents. In our research, we try to find a new modern and efficient psychological counseling mode to improve the mentality of parents and relieve their anxiety and depression. We divide guardians of parents into two groups .One group is given the traditional follow-up by regular phone call every month. The other is in a wechat group. A doctor send the useful information about kids care and answer questions of parents at regular time every month. The self-rating anxiety scale (SAS) and self-rating depression scale (SDS) scores of parents are marked before and after the long follow up.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2017

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

First Submitted

Initial submission to the registry

July 10, 2017

Completed
1 day until next milestone

Study Start

First participant enrolled

July 11, 2017

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 13, 2017

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2017

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 20, 2018

Completed
Last Updated

April 14, 2020

Status Verified

April 1, 2020

Enrollment Period

6 months

First QC Date

July 10, 2017

Last Update Submit

April 11, 2020

Conditions

Cataract

Keywords

congenital cataractanxietyguardian

Outcome Measures

Primary Outcomes (3)

  • similar effect

    the SAS and SDS level are same in two groups

    baseline

  • efficient effect

    the SAS and SDS level are higher in traditional group

    baseline

  • invalid effect

    the SAS and SDS level are lower in traditional group

    baseline

Study Arms (2)

traditional group

EXPERIMENTAL

phone call

Other: phone call

new device group

EXPERIMENTAL

wechat group

Other: wechat group

Interventions

phone callOTHER

Investigators give a regular follow-up to participants: phone call monthly

traditional group
wechat groupOTHER

Investigators give a regular follow-up to participants: wechat follow up. Investigators send useful information and answer their questions monthly.

new device group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may not qualify if:

  • have other major life hit was diagnosed of anxiety and depression before

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zhongshan Ophthalmic Center, Sun Yat-sen University

Guangzhou, Guangdong, 510000, China

Location

MeSH Terms

Conditions

CataractAnxiety Disorders

Condition Hierarchy (Ancestors)

Lens DiseasesEye DiseasesMental Disorders

Study Officials

  • Haotian Lin, M.D,Ph.D

    Zhongshan Ophthalmic Center, Sun Yat-sen University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator, Home for Cataract Children, Zhongshan Ophthalmic Center

Study Record Dates

First Submitted

July 10, 2017

First Posted

July 13, 2017

Study Start

July 11, 2017

Primary Completion

December 30, 2017

Study Completion

August 20, 2018

Last Updated

April 14, 2020

Record last verified: 2020-04

Locations

CN(1)