NCT00863031

Brief Summary

The aim of this study was to determine whether screening followed by brief PSC provided by primary care doctors could improve the quality of life of elderly patients with unrecognized psychological problems in primary care. The following hypotheses were tested:

  1. 1.Elderly patients screened positive of psychological problems had poorer health-related quality of life (HRQOL) than those who were screened negative.
  2. 2.Primary care doctors could be trained to provide brief PST.
  3. 3.Brief PST by a trained primary care doctor could improve the HRQOL of the elderly who were screened positive for psychological problems.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
299

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2002

Longer than P75 for not_applicable

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

November 1, 2002

Completed
3.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2005

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2006

Completed
2.8 years until next milestone

First Submitted

Initial submission to the registry

March 15, 2009

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 17, 2009

Completed
Last Updated

March 17, 2009

Status Verified

March 1, 2009

Enrollment Period

3.1 years

First QC Date

March 15, 2009

Last Update Submit

March 16, 2009

Conditions

Keywords

mental healthproblem-solving therapyelderlyhealth-related quality of lifeprimary careChinese

Outcome Measures

Primary Outcomes (1)

  • Health-related quality of life scores

    6, 12, 26 and 52 weeks

Secondary Outcomes (1)

  • Hospital Anxiety & Depression Scale scores

    6, 12, 26 and 52 weeks

Study Arms (2)

problem-solving therapy

EXPERIMENTAL

Three sessions of brief problem-solving counselling at week 1, 3 and 5 by a family doctor.

Behavioral: problem-solving therapy

viewing video

PLACEBO COMPARATOR

Three sessions of health education viewing video in groups of 3 to 5 people

Behavioral: Video-viewing

Interventions

Three sessions of problem-solving therapy at week 1, 3 and 5.

problem-solving therapy
Video-viewingBEHAVIORAL

Three sessions of viewing health educational videos.

viewing video

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Aged 60 or above
  • not known to have any psychological problem
  • HADS Depression score 6 or above, or Anxiety Score 3 or above
  • Written consent to study

You may not qualify if:

  • known psychological disease diagnosed by a registered doctor
  • history of taking any psychotropic drug prescribed by a registered doctor within the last year;
  • suicidal plan or strong suicidal thought;
  • psychotic symptom;
  • impairment in cognitive function; or
  • communication problem.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Two General Outpatient Clinics

Hong Kong, Hong Kong

Location

Related Publications (1)

  • Lam C.L.K., Lee P.W.H., Fong D.Y.T. and Lam T.P., A randomised controlled trial on the effectiveness of screening and brief problem-solving counselling for elderly patients with undiagnosed psychological problems in primary care., Hong Kong Medical Journal. HK Academy of Medicine Press, 2008, 14: 31-35.

    RESULT

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Cindy L.K. Lam, MD

    Family Medicine Unit, Faculty of Medicine, HKU

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 15, 2009

First Posted

March 17, 2009

Study Start

November 1, 2002

Primary Completion

December 1, 2005

Study Completion

June 1, 2006

Last Updated

March 17, 2009

Record last verified: 2009-03

Locations