The Study of the effectiveness of Group Quality of life Therapy on Pregnant Women

The Study of the effectiveness of Group Quality of life Therapy on Anxiety, Perceived Stress, General Health and Quality of life of Pregnant Women

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190620043956N1

Enrollment

Registered

2019-09-03

Start date

2017-02-19

Completion date

Unknown

Last updated

2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnant women.

Interventions

Intervention 1: Intervention group received Group Quality of Life Therapy based on Frisch Quality of Life Therapy during 8 sessions (weekly, 90 minutes, for 8 weeks). Intervention 2: Control group rec

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Pregnant women Reading and writing education Inclination to participat in research

Exclusion criteria

Exclusion criteria: Acute psychiatric disorders Unwillingness to complete the research process Get other psychological interventions

Design outcomes

Primary

Measure	Time frame
Quality of Life Score for Pregnant Women in the World Health Organization Quality of Life Questionnaire (2004). Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Measurement tools included the World Health Organization Quality of Life Questionnaire - Short Form (WHOQOL-BREF)(2004).	—

Measure

Time frame

Quality of Life Score for Pregnant Women in the World Health Organization Quality of Life Questionnaire (2004). Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Measurement tools included the World Health Organization Quality of Life Questionnaire - Short Form (WHOQOL-BREF)(2004).

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Secondary

Measure	Time frame
Anxiety. Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Instruments included beck anxiety inventory(1990).;Perceived Stress. Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Instruments included Cohen perceived stress questionnaire (1983).;General health. Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Instruments included Goldberg and Hiller general health questionnaire (1979).	—

Measure

Time frame

Anxiety. Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Instruments included beck anxiety inventory(1990).;Perceived Stress. Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Instruments included Cohen perceived stress questionnaire (1983).;General health. Timepoint: Measurements were performed at pre-test (Before the intervention), post-test (9 weeks after the intervention) and follow-up (15 weeks after the intervention). Method of measurement: Instruments included Goldberg and Hiller general health questionnaire (1979).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactNooshin Heidari

Islamic Azad University

nooshinheidari@yahoo.com+98 31 3535 4001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026