Feasibility and Efficacy of PRO-MAMAS

Tel Aviv University

Status: Invitation-only

Conditions: Chronic Stroke

Treatments: Behavioral: PRO-MAMAS (Promoting participation, health and wellbeing through meaningful maternal-role activities after stroke and other chronic conditions)

Study type: Interventional

Funder types: Other

Identifiers

NCT06895629

PRO-MAMAS 0010055-1

Details and patient eligibility

About

This experimental design will assess the feasibility & initial effectiveness of PRO-MAMAS (promoting participation, health and wellbeing through meaningful maternal-role activities after stroke and other chronic conditions) - a novel occupational therapy intervention program to promote participation, health and wellbeing of older mothers with chronic stroke.

Assessments will be conducted at three time points: baseline, pre, post the Pro-MAMA intervention

Full description

This study aims to test the feasibility and initial effectiveness of PRO-MAMAS (promoting participation, health and wellbeing through meaningful maternal-role activities after stroke and other chronic conditions) in improving participation, health and wellbeing among older community dwelling mothers with chronic stroke and other chronic conditions.

PRO-MAMAS is a group intervention that aims to promote the health and wellbeing of older mothers with chronic stroke and other chronic conditions by using meaningful maternal-role activities as a motivational mean for participation. The intervention will include group discussions and practice, analysis of facilitators and barriers for participation, and home exercise. PRO-MAMAS will focus on raising awareness to meaningful maternal-role activities, identifying facilitators and barriers for participation and problem solving to enhance meaningful participation.

Enrollment: 30 estimated patients

Sex: Female

Ages: 70 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Women
• Aged 70 and older
• Mothers (have at least one live and healthy child)
• With chronic stroke (at lease six months from stroke onset) or other age-related chronic conditions
• That live at home
• That they can walk independently (with or without a walking aid)
• Without significant cognitive decline (MoCA ≥19)

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

PRO-MAMAS

Experimental group

Description:

All participants will receive PRO-MAMAS - a novel occupational therapy intervention. PRO-MAMAS will include 8 sessions (2 sessions per week for 4 weeks). PRO-MAMAS will include small group of 5-8 participants, so approximately 4 rounds of PRO-MAMAS will be needed to reach 30 participants

Treatment:

Behavioral: PRO-MAMAS (Promoting participation, health and wellbeing through meaningful maternal-role activities after stroke and other chronic conditions)