Purpose in Life, Goals, and Expectations

April 27, 2026 updated by: Maureen C. Ashe, University of British Columbia

Purpose in Life, Goals, and Expectations of Older Adults After Hospitalization and Their Caregivers

Study investigators are inviting participants to participate in a study to describe older adults' and family caregivers' purpose in life, goals, and expectations for recovery after hospitalization. Study investigators will ask older adults and caregivers to take part in a telephone or online interview to ask questions and answer questionnaires related to their experience with the hospitalization.

Study Overview

Status

Withdrawn

Conditions

Study Type

Observational

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • British Columbia
      • Vancouver, British Columbia, Canada
        • The University of British Columbia

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Older adults 60y+ and family caregivers after hospitalization

Description

Inclusion Criteria:

  • Older adults 60y+ and family caregivers
  • after hospitalization

Exclusion Criteria:

  • We will exclude older adults with a dementia diagnosis, head injury, significant neurological impairment, not expected to live for 6 months or longer, or who receive treatment for medical conditions precluding enrolment.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Experience and perceptions after hospitalization
Time Frame: 1 day
Semi-structured interviews
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Falls Efficacy Scale-International (FES-I)
Time Frame: 1 day
A measure of a person's concern about falling. There are 16 items, each scored on a Likert scale with 1=not concerned and 4=very concerned. Higher scores indicate higher concerns fro falling.
1 day
Community Healthy Activities Model Program for Seniors (CHAMPS) Questionnaire
Time Frame: 1 day
Physical activity questionaire which records the frequency and duration of a person's activities
1 day
Life-Space questionnaire
Time Frame: 1 day
A measure of a person's mobility within their home, neighbourhood, and beyond (e.g., spatial movement). Participants respond yes/no to where they have been within the past 3 days (e..g., home, outside home in the neighborhood, etc.
1 day
Functional Independence Measure
Time Frame: 1 day
A measure of disability with a focus on self-care, transfers, walking, communication, and social cognition. It is an 18-item (7-level) ordinal scale. For each item (scored 1-7), the higher the score the more dependent the person is on the task.
1 day
Occupational Balance Questionnaire (Short form)
Time Frame: 1 day
Records the satisfaction with the amount and variation of a person's activities. It has 11 items with 4-step ordinal scales. Higher scores indicate higher occupational balance.
1 day
Telephone Interview for Cognitive Status (TICS) to screen for cognitive impairment
Time Frame: 1 day
A brief assessment of cognition for the telephone. There are 11 items, and the items are summed for a total TICS score. Results compared with previous dat at-scores and described qualitatively:Unimpaired, Ambiguous, Mildly Impaired, and Moderately to Severely Impaired
1 day
Hospital Anxiety and Depression Scale (HADS)
Time Frame: 1 day
Measures anxiety and depression in patients. There are 7 questions each for anxiety and depression. The lower the number indicate less anxiety/depression. For example, a score less than 7 is considered a "non-case". Scores range from 0-21.
1 day
Ryff Scales of Psychological Well-Being
Time Frame: 1 day
A 42-item scale which measures autonomy, environmental mastery, personal growth, positive relations with others, purpose in life, and self-acceptance. There are 42 statements using a 7-point scale (1 = strongly agree; 7 = strongly disagree). For overall score (all questions), higher scores suggest higher well-being.
1 day
EQ5D-5L
Time Frame: 1 day
A self-reported health related quality of life measure. There are 5 categories and the person chooses their responses based on categories, from no problems to extreme problems for each category (mobility, self-care, usual activities, pain, anxiety/depression. An index score is created out of 1; a higher index score the better. participants would also rate their health (0-100) with 100 as the best possible health. The higher the score the
1 day
ICECAP-O
Time Frame: 1 day
A self reported capability and well-being measure, with 5 attributes: attachment, security, role, enjoyment, and control. Index values out of 1, a higher value indicates higher reported capability and well-being.
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Maureen C Ashe, PhD, UBC

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

December 1, 2025

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

September 1, 2027

Study Registration Dates

First Submitted

July 11, 2022

First Submitted That Met QC Criteria

July 13, 2022

First Posted (Actual)

July 18, 2022

Study Record Updates

Last Update Posted (Actual)

May 1, 2026

Last Update Submitted That Met QC Criteria

April 27, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • H21-03607

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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