Effects of a Biopsychosocial-Spiritual Group Intervention on Quality of Life of Institutionalized Seniors

Mackay Medical College

Status: Completed

Conditions: Quality of Life

Treatments: Behavioral: the Biopsychosocial-Spiritual Group Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT05519280

MOST-105-2314-B-715-002-MY3

Details and patient eligibility

About

This study aimed to evaluate the effects of a biopsychosocial-spiritual (BPS-S) Group intervention on quality of life among seniors with disabilities in long-term care residential settings.

Full description

Background: Traditionally, biomedical care approach has been insufficient to meet the complex needs of older people living with multi-morbidity. Promoting whole-person wellness and better quality of life becomes a key goal of care in residential long-term care facilities. The integrative approaches composed of physio-psycho-social and spiritual components might be a viable strategy to assist older adults accept uncontrollable life changes and enhance holistic wellness.

Purpose: The study purpose was to develop and evaluate the effects of 8-week biopsychosocial-spiritual (BPS-S) group intervention versus usual care on self-perception of quality of life (QoL) and meaning in life among seniors with disability in residential care home at mid- and post-intervention, and at a 1-month follow up.

Methods: This single-blind randomized controlled trail with repeated measures design was conducted in residential long-term care facilities. Both the experimental groups (EG) and the control group (CG) received routing group activities based on their institution's schedule. Additionally, the EG received 8 sessions of weekly BPS-S group therapy for 80 minutes each. The baseline characteristics of residents with disabilities (including demographic information, length of stay in the institution and medical conditions) were collected using a data sheet, and activities of daily living of these residents were measured using the Barthel Index. To evaluate the effectiveness of the BPS-S group therapy, the primary outcomes including "participants' overall QOL" and the secondary outcome "meaning in life" were assessed at four time points: before, mid- and post- intervention and at a 1-month follow up. Quality of Life Index (QLI)-Part I and Purpose in Life (PIL) test were used to measure these outcome variables, respectively.

Enrollment: 83 patients

Sex: All

Ages: 65 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. being 65 years of age or older;
2. living in the institution for at least 1 month;
3. Barthel Index scores under 90;
4. no hearing, visual impairment and infectious diseases;
5. being able to follow instructions and participate in group activities.

Exclusion criteria

have the diagnosis of major depression.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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83 participants in 2 patient groups

the Biopsychosocial-Spiritual Group Intervention

Experimental group

Description:

The experimental group received 8 sessions of weekly BPS-S group therapy for 80 minutes each.

Treatment:

Behavioral: the Biopsychosocial-Spiritual Group Intervention

weekly general chatting activities

No Intervention group

Description:

The Control group received weekly general chatting activities for 30 minutes.